Canonical Allele Identifier: CA1149683790
Gene:

Linked Data

dbSNP Id: rs1020437691

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2567442G>T , CM000663.2:g.2567442G>T GRCh38
NC_000001.10:g.2498881G>T , CM000663.1:g.2498881G>T GRCh37
NC_000001.9:g.2475537C>A NCBI36
NG_047096.1:g.16078G>T

Transcript Alleles

HGVS Amino-acid Change
NR_121638.1:n.71+837G>T