Canonical Allele Identifier: CA93117888
Gene:

Linked Data

dbSNP Id: rs1008239094
gnomAD v2: 4-12579661-A-G
gnomAD v3: 4-12578037-A-G
gnomAD v4: 4-12578037-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578037A>G , CM000666.2:g.12578037A>G GRCh38
NC_000004.11:g.12579661A>G , CM000666.1:g.12579661A>G GRCh37
NC_000004.10:g.12188759A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_925406.1:n.106+31305T>C
XR_001741374.1:n.254+44618T>C
XR_925406.3:n.140+31305T>C