Canonical Allele Identifier: CA860367900
Gene:

Linked Data

dbSNP Id: rs1333183874

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.129576855A>G , CM000671.2:g.129576855A>G GRCh38
NC_000009.11:g.132339134A>G , CM000671.1:g.132339134A>G GRCh37
NC_000009.10:g.131378955A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930390.1:n.182+1257A>G