Canonical Allele Identifier: CA1929213282
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762462C= , CM000672.2:g.94762462C= GRCh38
NC_000010.10:g.96522219C= , CM000672.1:g.96522219C= GRCh37
NC_000010.9:g.96512209C= NCBI36
NG_008384.2:g.4757C=
NG_008384.3:g.4782C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000464755.1:c.932-12596C= ENSP00000483243.1:n.932-12596C=