Canonical Allele Identifier: CA674019867
Gene: CALCB HGNC NCBI

Linked Data

dbSNP Id: rs1225698063
gnomAD v3: 11-14972887-C-T
gnomAD v4: 11-14972887-C-T
MyVariant Identifiers: chr11:g.14972887C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.14972887C>T , CM000673.2:g.14972887C>T GRCh38
NC_000011.9:g.14994433C>T , CM000673.1:g.14994433C>T GRCh37
NC_000011.8:g.14951009C>T NCBI36
NG_015960.1:g.4400G>A , LRG_13:g.4400G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000523376.5:c.-445-5004C>T ENSP00000428882.1:n.-445-5004C>T
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