Canonical Allele Identifier: CA1929213289
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762466C= , CM000672.2:g.94762466C= GRCh38
NC_000010.10:g.96522223C= , CM000672.1:g.96522223C= GRCh37
NC_000010.9:g.96512213C= NCBI36
NG_008384.2:g.4761C=
NG_008384.3:g.4786C=

Transcript Alleles

HGVS Amino-acid change
ENST00000464755.1:c.932-12592C= ENSP00000483243.1:n.932-12592C=