Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
A/T | Ancestral: A | Ambiguity code: W
Location

Chromosome 2:26466723 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM990991

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 11 HGVS names - click the plus to show

2:g.26466723A>T
ENST00000403946.5:c.4491T>A
ENSP00000385255.3:p.Tyr1497Ter
ENST00000338581.8:c.2190T>A
ENSP00000345137.6:p.Tyr730Ter
ENST00000272371.4:c.4491T>A
ENSP00000272371.2:p.Tyr1497Ter
ENST00000339598.5:c.2190T>A
ENSP00000344521.3:p.Tyr730Ter
ENST00000402415.5:c.2421T>A
ENSP00000383906.3:p.Tyr807Ter

Variation displays