Canonical Allele Identifier: CA1929213454
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762605C= , CM000672.2:g.94762605C= GRCh38
NC_000010.10:g.96522362C= , CM000672.1:g.96522362C= GRCh37
NC_000010.9:g.96512352C= NCBI36
NG_008384.2:g.4900C=
NG_008384.3:g.4925C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000464755.1:c.932-12453C= ENSP00000483243.1:n.932-12453C=