Canonical Allele Identifier: CA786695559
Gene:

Linked Data

dbSNP Id: rs1306814671
gnomAD v3: 4-12578277-C-A
gnomAD v4: 4-12578277-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578277C>A , CM000666.2:g.12578277C>A GRCh38
NC_000004.11:g.12579901C>A , CM000666.1:g.12579901C>A GRCh37
NC_000004.10:g.12188999C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_925406.1:n.106+31065G>T
XR_001741374.1:n.254+44378G>T
XR_925406.3:n.140+31065G>T