Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 5:37014728 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM042513

Most severe consequence
Clinical significance

Synonyms

LSDB 15889

This variation has 6 HGVS names - click the plus to show

5:g.37014728C>T
ENST00000448238.2:c.4606C>T
ENSP00000406266.2:p.Arg1536Ter
ENST00000621733.1:c.1-49850C>T
ENST00000282516.10:c.4606C>T
ENSP00000282516.8:p.Arg1536Ter

Variation displays