Canonical Allele Identifier: CA93117898
Gene:

Linked Data

dbSNP Id: rs1006999208
gnomAD v2: 4-12579734-T-C
gnomAD v3: 4-12578110-T-C
gnomAD v4: 4-12578110-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578110T>C , CM000666.2:g.12578110T>C GRCh38
NC_000004.11:g.12579734T>C , CM000666.1:g.12579734T>C GRCh37
NC_000004.10:g.12188832T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_925406.1:n.106+31232A>G
XR_001741374.1:n.254+44545A>G
XR_925406.3:n.140+31232A>G