Canonical Allele Identifier: CA93117928
Gene:

Linked Data

dbSNP Id: rs971307994
gnomAD v2: 4-12579935-C-T
gnomAD v3: 4-12578311-C-T
gnomAD v4: 4-12578311-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578311C>T , CM000666.2:g.12578311C>T GRCh38
NC_000004.11:g.12579935C>T , CM000666.1:g.12579935C>T GRCh37
NC_000004.10:g.12189033C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_925406.1:n.106+31031G>A
XR_001741374.1:n.254+44344G>A
XR_925406.3:n.140+31031G>A