Canonical Allele Identifier: CA93117895
Gene:

Linked Data

dbSNP Id: rs1003842000
gnomAD v3: 4-12578090-G-A
gnomAD v4: 4-12578090-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578090G>A , CM000666.2:g.12578090G>A GRCh38
NC_000004.11:g.12579714G>A , CM000666.1:g.12579714G>A GRCh37
NC_000004.10:g.12188812G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_925406.1:n.106+31252C>T
XR_001741374.1:n.254+44565C>T
XR_925406.3:n.140+31252C>T