Canonical Allele Identifier: CA1284674190
Gene:

Linked Data

dbSNP Id: rs1680374599

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122884045T>C , CM000664.2:g.122884045T>C GRCh38
NC_000002.11:g.123641621T>C , CM000664.1:g.123641621T>C GRCh37
NC_000002.10:g.123358091T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923292.1:n.1125-897T>C
XR_001739692.1:n.1451-897T>C
XR_923292.2:n.1358-897T>C