Canonical Allele Identifier: CA1954016349
Gene: CALCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.14972907C= , CM000673.2:g.14972907C= GRCh38
NC_000011.9:g.14994453C= , CM000673.1:g.14994453C= GRCh37
NC_000011.8:g.14951029C= NCBI36
NG_015960.1:g.4380G= , LRG_13:g.4380G=

Transcript Alleles

HGVS Amino-acid change
ENST00000523376.5:c.-445-4984C= ENSP00000428882.1:n.-445-4984C=