Canonical Allele Identifier: CA1481405930
Gene:

Linked Data

dbSNP Id: rs1578687815

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102500001G>C , CM000666.2:g.102500001G>C GRCh38
NC_000004.11:g.103421158G>C , CM000666.1:g.103421158G>C GRCh37
NC_000004.10:g.103640190G>C NCBI36
NG_050628.1:g.3673G>C

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+1248C>G XP_011530769.1:n.643+1248C>G
NR_136202.1:n.48+2438C>G