Canonical Allele Identifier: CA93117920
Gene:

Linked Data

dbSNP Id: rs1016712225

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578251A>G , CM000666.2:g.12578251A>G GRCh38
NC_000004.11:g.12579875A>G , CM000666.1:g.12579875A>G GRCh37
NC_000004.10:g.12188973A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_925406.1:n.106+31091T>C
XR_001741374.1:n.254+44404T>C
XR_925406.3:n.140+31091T>C