Canonical Allele Identifier: CA218216144
Gene: CALCB HGNC NCBI

Linked Data

dbSNP Id: rs531410453

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.14972926G>A , CM000673.2:g.14972926G>A GRCh38
NC_000011.9:g.14994472G>A , CM000673.1:g.14994472G>A GRCh37
NC_000011.8:g.14951048G>A NCBI36
NG_015960.1:g.4361C>T , LRG_13:g.4361C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000523376.5:c.-445-4965G>A ENSP00000428882.1:n.-445-4965G>A