Canonical Allele Identifier: CA191701680
Gene:

Linked Data

dbSNP Id: rs1044191193

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551221G>C , CM000671.2:g.25551221G>C GRCh38
NC_000009.11:g.25551219G>C , CM000671.1:g.25551219G>C GRCh37
NC_000009.10:g.25541219G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_929525.1:n.50-649C>G
XR_929525.2:n.674-649C>G