Canonical Allele Identifier: CA1827744309
Gene:

Linked Data

dbSNP Id: rs1817920415

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.1787546T>C , CM000671.2:g.1787546T>C GRCh38
NC_000009.11:g.1787546T>C , CM000671.1:g.1787546T>C GRCh37
NC_000009.10:g.1777546T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001746599.1:n.142+68634T>C