Canonical Allele Identifier: CA2580859172
Gene:

Linked Data

dbSNP Id: rs10974531

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.4426631C>T , CM000671.2:g.4426631C>T GRCh38
NC_000009.11:g.4426631C>T , CM000671.1:g.4426631C>T GRCh37
NC_000009.10:g.4416631C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_929447.1:n.192+4778G>A