Canonical Allele Identifier: CA1929213285
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762464A= , CM000672.2:g.94762464A= GRCh38
NC_000010.10:g.96522221A= , CM000672.1:g.96522221A= GRCh37
NC_000010.9:g.96512211A= NCBI36
NG_008384.2:g.4759A=
NG_008384.3:g.4784A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000464755.1:c.932-12594A= ENSP00000483243.1:n.932-12594A=