Canonical Allele Identifier: CA1954016361
Gene: CALCB HGNC NCBI

Linked Data

dbSNP Id: rs1849640852

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.14972930G>C , CM000673.2:g.14972930G>C GRCh38
NC_000011.9:g.14994476G>C , CM000673.1:g.14994476G>C GRCh37
NC_000011.8:g.14951052G>C NCBI36
NG_015960.1:g.4357C>G , LRG_13:g.4357C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000523376.5:c.-445-4961G>C ENSP00000428882.1:n.-445-4961G>C