Canonical Allele Identifier: CA2700257441
Gene:

Linked Data

dbSNP Id: rs2104565204

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.120331878G>A , CM000664.2:g.120331878G>A GRCh38
NC_000002.11:g.121089454G>A , CM000664.1:g.121089454G>A GRCh37
NC_000002.10:g.120805924G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011512307.1:c.141+3072G>A XP_011510609.1:n.141+3072G>A