Canonical Allele Identifier: CA2025046527
Gene:

Linked Data

dbSNP Id: rs1944932289

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.29961033G>T , CM000674.2:g.29961033G>T GRCh38
NC_000012.11:g.30113966G>T , CM000674.1:g.30113966G>T GRCh37
NC_000012.10:g.30005233G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_931473.1:n.314-17993C>A
XR_931474.1:n.314-17993C>A
XR_931475.1:n.135-17993C>A
XR_001749060.1:n.314-17993C>A
XR_001749061.1:n.314-17993C>A