Canonical Allele Identifier: CA1954016346
Gene: CALCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.14972896T= , CM000673.2:g.14972896T= GRCh38
NC_000011.9:g.14994442T= , CM000673.1:g.14994442T= GRCh37
NC_000011.8:g.14951018T= NCBI36
NG_015960.1:g.4391A= , LRG_13:g.4391A=

Transcript Alleles

HGVS Amino-acid change
ENST00000523376.5:c.-445-4995T= ENSP00000428882.1:n.-445-4995T=