Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R
Location

Chromosome 2:26475453 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM053367

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.26475453A>G
ENST00000403946.4:c.3032T>C
ENSP00000385255.3:p.Leu1011Pro
ENST00000338581.7:c.791T>C
ENSP00000345137.6:p.Leu264Pro
ENST00000272371.3:c.3032T>C
ENSP00000272371.2:p.Leu1011Pro
ENST00000339598.4:c.791T>C
ENSP00000344521.3:p.Leu264Pro
ENST00000402415.4:c.962T>C
ENSP00000383906.3:p.Leu321Pro

Variation displays