Canonical Allele Identifier: CA13023559
Gene:

Identifiers and link-outs to other resources

dbSNP Id: rs10812641

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2777384T>A , CM000671.2:g.2777384T>A GRCh38
NC_000009.11:g.2777384T>A , CM000671.1:g.2777384T>A GRCh37
NC_000009.10:g.2767384T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000490444.2:n.276+5372A>T ENSP00000474467.1:p.=