Canonical Allele Identifier: CA1929213293
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762469G= , CM000672.2:g.94762469G= GRCh38
NC_000010.10:g.96522226G= , CM000672.1:g.96522226G= GRCh37
NC_000010.9:g.96512216G= NCBI36
NG_008384.2:g.4764G=
NG_008384.3:g.4789G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000464755.1:c.932-12589G= ENSP00000483243.1:n.932-12589G=