Canonical Allele Identifier: CA2700308948
Gene:

Linked Data

dbSNP Id: rs2104659790

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122884019T>C , CM000664.2:g.122884019T>C GRCh38
NC_000002.11:g.123641595T>C , CM000664.1:g.123641595T>C GRCh37
NC_000002.10:g.123358065T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923292.1:n.1125-923T>C
XR_001739692.1:n.1451-923T>C
XR_923292.2:n.1358-923T>C