Canonical Allele Identifier: CA2210126476
Gene:

Linked Data

dbSNP Id: rs1883222329

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16143846G>A , CM000678.2:g.16143846G>A GRCh38
NC_000016.9:g.16237703G>A , CM000678.1:g.16237703G>A GRCh37
NC_000016.8:g.16145204G>A NCBI36
NG_028268.1:g.199270G>A
NG_028268.2:g.199270G>A

Transcript Alleles

HGVS Amino-acid change
XR_933134.1:n.94G>A