Canonical Allele Identifier: CA1929213422
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762582T= , CM000672.2:g.94762582T= GRCh38
NC_000010.10:g.96522339T= , CM000672.1:g.96522339T= GRCh37
NC_000010.9:g.96512329T= NCBI36
NG_008384.2:g.4877T=
NG_008384.3:g.4902T=

Transcript Alleles

HGVS Amino-acid change
ENST00000464755.1:c.932-12476T= ENSP00000483243.1:n.932-12476T=