Canonical Allele Identifier: CA1979711957
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66510582A= , CM000673.2:g.66510582A= GRCh38
NC_000011.9:g.66278053A= , CM000673.1:g.66278053A= GRCh37
NC_000011.8:g.66034629A= NCBI36
NG_009093.1:g.4935A=
NG_032068.1:g.35174A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000419755.3:c.159-431A= ENSP00000398526.3:n.159-431A=