Canonical Allele Identifier: CA1481405732
Gene:

Linked Data

dbSNP Id: rs1738883604

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102499813G>C , CM000666.2:g.102499813G>C GRCh38
NC_000004.11:g.103420970G>C , CM000666.1:g.103420970G>C GRCh37
NC_000004.10:g.103640002G>C NCBI36
NG_050628.1:g.3485G>C

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+1436C>G XP_011530769.1:n.643+1436C>G
NR_136202.1:n.48+2626C>G