Canonical Allele Identifier: CA1840046589
Gene:

Linked Data

dbSNP Id: rs10511729

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.23557229T>A , CM000671.2:g.23557229T>A GRCh38
NC_000009.11:g.23557227T>A , CM000671.1:g.23557227T>A GRCh37
NC_000009.10:g.23547227T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121602.1:n.1847-2612A>T