Canonical Allele Identifier: CA1096565481
Gene:

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160668802T>G , CM000668.2:g.160668802T>G GRCh38
NC_000006.11:g.161089834T>G , CM000668.1:g.161089834T>G GRCh37
NC_000006.10:g.161009824T>G NCBI36
NG_016147.1:g.2574A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000452651.1:n.115-2429A>C