Canonical Allele Identifier: CA2792482563
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66510585C>G , CM000673.2:g.66510585C>G GRCh38
NC_000011.9:g.66278056C>G , CM000673.1:g.66278056C>G GRCh37
NC_000011.8:g.66034632C>G NCBI36
NG_009093.1:g.4938C>G
NG_032068.1:g.35177C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000419755.3:c.159-428C>G ENSP00000398526.3:n.159-428C>G