Canonical Allele Identifier: CA674019892
Gene: CALCB HGNC NCBI

Linked Data

dbSNP Id: rs1428101482
MyVariant Identifiers: chr11:g.14972919A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.14972919A>G , CM000673.2:g.14972919A>G GRCh38
NC_000011.9:g.14994465A>G , CM000673.1:g.14994465A>G GRCh37
NC_000011.8:g.14951041A>G NCBI36
NG_015960.1:g.4368T>C , LRG_13:g.4368T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000523376.5:c.-445-4972A>G ENSP00000428882.1:n.-445-4972A>G