Canonical Allele Identifier: CA1880834354
Gene:

Linked Data

dbSNP Id: rs1588095026

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.129576821C>T , CM000671.2:g.129576821C>T GRCh38
NC_000009.11:g.132339100C>T , CM000671.1:g.132339100C>T GRCh37
NC_000009.10:g.131378921C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930390.1:n.182+1223C>T