Canonical Allele Identifier: CA1149683793
Gene:

Linked Data

dbSNP Id: rs1644376623

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2567446G>C , CM000663.2:g.2567446G>C GRCh38
NC_000001.10:g.2498885G>C , CM000663.1:g.2498885G>C GRCh37
NC_000001.9:g.2475533C>G NCBI36
NG_047096.1:g.16082G>C

Transcript Alleles

HGVS Amino-acid Change
NR_121638.1:n.71+841G>C