Canonical Allele Identifier: CA786695563
Gene:

Linked Data

dbSNP Id: rs1413784735

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578283A>C , CM000666.2:g.12578283A>C GRCh38
NC_000004.11:g.12579907A>C , CM000666.1:g.12579907A>C GRCh37
NC_000004.10:g.12189005A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_925406.1:n.106+31059T>G
XR_001741374.1:n.254+44372T>G
XR_925406.3:n.140+31059T>G