Canonical Allele Identifier: CA471499477
Gene: CALHM1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.105218140T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.103458383T>C , CM000672.2:g.103458383T>C GRCh38
NC_000010.10:g.105218140T>C , CM000672.1:g.105218140T>C GRCh37
NC_000010.9:g.105208130T>C NCBI36
NG_016855.1:g.5509A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000329905.6:c.369A>G MANE Select ENSP00000329926.6:p.Lys123=
ENST00000329905.5:c.369A>G ENSP00000329926.5:p.Lys123=
NM_001001412.3:c.369A>G NP_001001412.3:p.Lys123=
NM_001001412.4:c.369A>G MANE Select NP_001001412.3:p.Lys123=
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