Canonical Allele Identifier: CA1929213332
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762517C= , CM000672.2:g.94762517C= GRCh38
NC_000010.10:g.96522274C= , CM000672.1:g.96522274C= GRCh37
NC_000010.9:g.96512264C= NCBI36
NG_008384.2:g.4812C=
NG_008384.3:g.4837C=

Transcript Alleles

HGVS Amino-acid change
ENST00000464755.1:c.932-12541C= ENSP00000483243.1:n.932-12541C=