Canonical Allele Identifier: CA2710977698
Gene:

Linked Data

dbSNP Id: rs2113482180

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.11943516T>G , CM000668.2:g.11943516T>G GRCh38
NC_000006.11:g.11943749T>G , CM000668.1:g.11943749T>G GRCh37
NC_000006.10:g.12051735T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001743976.1:n.348-8019T>G