Canonical Allele Identifier: CA1458504820
Gene:

Linked Data

dbSNP Id: rs1720484273

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.54228490G>A , CM000666.2:g.54228490G>A GRCh38
NC_000004.11:g.55094657G>A , CM000666.1:g.55094657G>A GRCh37
NC_000004.10:g.54789414G>A NCBI36
NG_009250.1:g.4394G>A , LRG_309:g.4394G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000507166.5:c.1018-46435G>A ENSP00000423325.1:n.1018-46435G>A