Canonical Allele Identifier: CA1354756214
Gene:

Linked Data

dbSNP Id: rs1695461363

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30420891C>G , CM000665.2:g.30420891C>G GRCh38
NC_000003.11:g.30462383C>G , CM000665.1:g.30462383C>G GRCh37
NC_000003.10:g.30437387C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940686.1:n.1367+29003C>G
XR_940687.1:n.1415+29003C>G
XR_001740627.1:n.801+29003C>G
XR_001740628.1:n.849+29003C>G
XR_427322.3:n.802-15302C>G
XR_940683.2:n.1769G>C