Canonical Allele Identifier: CA307575806
Gene:

Linked Data

dbSNP Id: rs896839472

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33521939G>A , CM000681.2:g.33521939G>A GRCh38
NC_000019.9:g.34012845G>A , CM000681.1:g.34012845G>A GRCh37
NC_000019.8:g.38704685G>A NCBI36
NG_013358.1:g.4955C>T
NG_013358.2:g.4955C>T

Transcript Alleles

HGVS Amino-acid Change
XR_001754035.2:n.6G>A
XR_935918.2:n.6G>A