Canonical Allele Identifier: CA2713612099
Gene:

Linked Data

dbSNP Id: rs2114807757

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.163765604C>G , CM000668.2:g.163765604C>G GRCh38
NC_000006.11:g.164186636C>G , CM000668.1:g.164186636C>G GRCh37
NC_000006.10:g.164106626C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001744452.1:n.410+6175C>G
XR_001744454.1:n.369+6216C>G
XR_001744455.1:n.346+6239C>G