Canonical Allele Identifier: CA1929213268
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762440T= , CM000672.2:g.94762440T= GRCh38
NC_000010.10:g.96522197T= , CM000672.1:g.96522197T= GRCh37
NC_000010.9:g.96512187T= NCBI36
NG_008384.2:g.4735T=
NG_008384.3:g.4760T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000464755.1:c.932-12618T= ENSP00000483243.1:n.932-12618T=