Canonical Allele Identifier: CA786695546
Gene:

Linked Data

dbSNP Id: rs1246593460

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578196A>G , CM000666.2:g.12578196A>G GRCh38
NC_000004.11:g.12579820A>G , CM000666.1:g.12579820A>G GRCh37
NC_000004.10:g.12188918A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_925406.1:n.106+31146T>C
XR_001741374.1:n.254+44459T>C
XR_925406.3:n.140+31146T>C