Canonical Allele Identifier: CA2580598881
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762608T>A , CM000672.2:g.94762608T>A GRCh38
NC_000010.10:g.96522365T>A , CM000672.1:g.96522365T>A GRCh37
NC_000010.9:g.96512355T>A NCBI36
NG_008384.2:g.4903T>A
NG_008384.3:g.4928T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000464755.1:c.932-12450T>A ENSP00000483243.1:n.932-12450T>A