Canonical Allele Identifier: CA1954016338
Gene: CALCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.14972881_14972883delinsGGA , CM000673.2:g.14972881_14972883delinsGGA GRCh38
NC_000011.9:g.14994427_14994429delinsGGA , CM000673.1:g.14994427_14994429delinsGGA GRCh37
NC_000011.8:g.14951003_14951005delinsGGA NCBI36
NG_015960.1:g.4404_4406delinsTCC , LRG_13:g.4404_4406delinsTCC

Transcript Alleles

HGVS Amino-acid change
ENST00000523376.5:c.-445-5010_-445-5008delinsGGA ENSP00000428882.1:n.-445-5010_-445-5008delinsGGA