Canonical Allele Identifier: CA1954016352
Gene: CALCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.14972912T= , CM000673.2:g.14972912T= GRCh38
NC_000011.9:g.14994458T= , CM000673.1:g.14994458T= GRCh37
NC_000011.8:g.14951034T= NCBI36
NG_015960.1:g.4375A= , LRG_13:g.4375A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000523376.5:c.-445-4979T= ENSP00000428882.1:n.-445-4979T=