Canonical Allele Identifier: CA1954016341
Gene: CALCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.14972889A= , CM000673.2:g.14972889A= GRCh38
NC_000011.9:g.14994435A= , CM000673.1:g.14994435A= GRCh37
NC_000011.8:g.14951011A= NCBI36
NG_015960.1:g.4398T= , LRG_13:g.4398T=

Transcript Alleles

HGVS Amino-acid change
ENST00000523376.5:c.-445-5002A= ENSP00000428882.1:n.-445-5002A=