Canonical Allele Identifier: CA2723068416
Gene: CALCB HGNC NCBI

Linked Data

dbSNP Id: rs531410453
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.14972926G>T , CM000673.2:g.14972926G>T GRCh38
NC_000011.9:g.14994472G>T , CM000673.1:g.14994472G>T GRCh37
NC_000011.8:g.14951048G>T NCBI36
NG_015960.1:g.4361C>A , LRG_13:g.4361C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000523376.5:c.-445-4965G>T ENSP00000428882.1:n.-445-4965G>T
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