Canonical Allele Identifier: CA1677169865
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160668432C= , CM000668.2:g.160668432C= GRCh38
NC_000006.11:g.161089464C= , CM000668.1:g.161089464C= GRCh37
NC_000006.10:g.161009454C= NCBI36
NG_016147.1:g.2944G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000452651.1:n.115-2059G=