Canonical Allele Identifier: CA1954016334
Gene: CALCB HGNC NCBI

Linked Data

dbSNP Id: rs1590269769
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.14972878A>G , CM000673.2:g.14972878A>G GRCh38
NC_000011.9:g.14994424A>G , CM000673.1:g.14994424A>G GRCh37
NC_000011.8:g.14951000A>G NCBI36
NG_015960.1:g.4409T>C , LRG_13:g.4409T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000523376.5:c.-445-5013A>G ENSP00000428882.1:n.-445-5013A>G
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