Canonical Allele Identifier: CA1605795016
Gene:

Linked Data

dbSNP Id: rs1761316353

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1535672G>A , CM000668.2:g.1535672G>A GRCh38
NC_000006.11:g.1535907G>A , CM000668.1:g.1535907G>A GRCh37
NC_000006.10:g.1480906G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_427861.2:n.234+16674C>T
XR_926380.1:n.218-2784G>A
XR_926381.1:n.1108-2784G>A
XR_926382.1:n.235-6493C>T
XR_926384.1:n.200-6493C>T
XR_001743921.1:n.235-6517C>T
XR_427861.3:n.234+16674C>T
XR_926381.2:n.1123-2784G>A