Canonical Allele Identifier: CA935379646

Gene: CALCB

Linked Data

• dbSNP Id: rs1849640234
• gnomAD v3: 11-14972910-G-A
• gnomAD v4: 11-14972910-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.14972910G>A , CM000673.2:g.14972910G>A	GRCh38
NC_000011.9:g.14994456G>A , CM000673.1:g.14994456G>A	GRCh37
NC_000011.8:g.14951032G>A	NCBI36
NG_015960.1:g.4377C>T , LRG_13:g.4377C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000523376.5:c.-445-4981G>A	ENSP00000428882.1:n.-445-4981G>A