Canonical Allele Identifier: CA193944079
Gene:

Identifiers and link-outs to other resources

dbSNP Id: rs11143005

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.68578354G>T , CM000671.2:g.68578354G>T GRCh38
NC_000009.10:g.70383090G>T NCBI36
NC_000009.11:g.71193270G>T , CM000671.1:g.71193270G>T GRCh37

Transcript Alleles

HGVS Amino-acid change
XR_929903.1:n.449+35712G>T