Canonical Allele Identifier: CA935379650

Gene: CALCB

Linked Data

• dbSNP Id: rs1849640534
• gnomAD v3: 11-14972916-G-A
• gnomAD v4: 11-14972916-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.14972916G>A , CM000673.2:g.14972916G>A	GRCh38
NC_000011.9:g.14994462G>A , CM000673.1:g.14994462G>A	GRCh37
NC_000011.8:g.14951038G>A	NCBI36
NG_015960.1:g.4371C>T , LRG_13:g.4371C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000523376.5:c.-445-4975G>A	ENSP00000428882.1:n.-445-4975G>A