Canonical Allele Identifier: CA1149683786
Gene:

Linked Data

dbSNP Id: rs1183226320

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2567439G>A , CM000663.2:g.2567439G>A GRCh38
NC_000001.10:g.2498878G>A , CM000663.1:g.2498878G>A GRCh37
NC_000001.9:g.2475540C>T NCBI36
NG_047096.1:g.16075G>A

Transcript Alleles

HGVS Amino-acid Change
NR_121638.1:n.71+834G>A