Canonical Allele Identifier: CA1839056691
Gene:

Linked Data

dbSNP Id: rs1823377723

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21755994T>C , CM000671.2:g.21755994T>C GRCh38
NC_000009.11:g.21755993T>C , CM000671.1:g.21755993T>C GRCh37
NC_000009.10:g.21745993T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001746563.2:n.163+11831A>G