Canonical Allele Identifier: CA1175223529
Gene:

Linked Data

dbSNP Id: rs1656869631

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.72299371C>T , CM000663.2:g.72299371C>T GRCh38
NC_000001.10:g.72765054C>T , CM000663.1:g.72765054C>T GRCh37
NC_000001.9:g.72537642C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_947505.1:n.310+15966C>T
XR_947506.1:n.310+15966C>T
XR_947507.1:n.310+15966C>T
XR_001737670.1:n.414+15966C>T
XR_001737671.2:n.418+15966C>T
XR_947505.2:n.414+15966C>T
XR_947506.2:n.414+15966C>T