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 5:37057211 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM041506

Most severe consequence
Clinical significance

Synonyms

LSDB 15879

This variation has 7 HGVS names - click the plus to show

5:g.37057211A>G
ENST00000514335.1:n.1171A>G
ENST00000448238.2:c.7289A>G
ENSP00000406266.2:p.Tyr2430Cys
ENST00000621733.1:c.1-7367A>G
ENST00000282516.9:c.7289A>G
ENSP00000282516.8:p.Tyr2430Cys

Variation displays