Canonical Allele Identifier: CA2501063383
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160668585A>G , CM000668.2:g.160668585A>G GRCh38
NC_000006.11:g.161089617A>G , CM000668.1:g.161089617A>G GRCh37
NC_000006.10:g.161009607A>G NCBI36
NG_016147.1:g.2791T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000452651.1:n.115-2212T>C