Canonical Allele Identifier: CA1929213272
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762448C= , CM000672.2:g.94762448C= GRCh38
NC_000010.10:g.96522205C= , CM000672.1:g.96522205C= GRCh37
NC_000010.9:g.96512195C= NCBI36
NG_008384.2:g.4743C=
NG_008384.3:g.4768C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000464755.1:c.932-12610C= ENSP00000483243.1:n.932-12610C=