Canonical Allele Identifier: CA1149683775
Gene:

Linked Data

dbSNP Id: rs1644376491

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2567425C>G , CM000663.2:g.2567425C>G GRCh38
NC_000001.10:g.2498864C>G , CM000663.1:g.2498864C>G GRCh37
NC_000001.9:g.2475554G>C NCBI36
NG_047096.1:g.16061C>G

Transcript Alleles

HGVS Amino-acid Change
NR_121638.1:n.71+820C>G