Canonical Allele Identifier: CA1839056651
Gene:

Linked Data

dbSNP Id: rs1587158555

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21755925C>A , CM000671.2:g.21755925C>A GRCh38
NC_000009.11:g.21755924C>A , CM000671.1:g.21755924C>A GRCh37
NC_000009.10:g.21745924C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001746563.2:n.163+11900G>T