Canonical Allele Identifier: CA1284436097
Gene:

Linked Data

dbSNP Id: rs1573711190

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122379288T>A , CM000664.2:g.122379288T>A GRCh38
NC_000002.11:g.123136864T>A , CM000664.1:g.123136864T>A GRCh37
NC_000002.10:g.122853334T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923278.1:n.556-13675T>A
XR_001739684.1:n.556-13675T>A