Canonical Allele Identifier: CA1979711960
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66510587C= , CM000673.2:g.66510587C= GRCh38
NC_000011.9:g.66278058C= , CM000673.1:g.66278058C= GRCh37
NC_000011.8:g.66034634C= NCBI36
NG_009093.1:g.4940C=
NG_032068.1:g.35179C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000419755.3:c.159-426C= ENSP00000398526.3:n.159-426C=