Canonical Allele Identifier: CA674019887
Gene: CALCB HGNC NCBI

Linked Data

dbSNP Id: rs1325443175
MyVariant Identifiers: chr11:g.14972907C>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000523376.5:c.-445-4984C>G ENSP00000428882.1:n.-445-4984C>G