Canonical Allele Identifier: CA1827744273
Gene:

Linked Data

dbSNP Id: rs1817919806

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.1787491T>C , CM000671.2:g.1787491T>C GRCh38
NC_000009.11:g.1787491T>C , CM000671.1:g.1787491T>C GRCh37
NC_000009.10:g.1777491T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001746599.1:n.142+68579T>C