Canonical Allele Identifier: CA471499583
Gene: CALHM1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.105218065A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.103458308A>T , CM000672.2:g.103458308A>T GRCh38
NC_000010.10:g.105218065A>T , CM000672.1:g.105218065A>T GRCh37
NC_000010.9:g.105208055A>T NCBI36
NG_016855.1:g.5584T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000329905.6:c.444T>A MANE Select ENSP00000329926.6:p.Pro148=
ENST00000329905.5:c.444T>A ENSP00000329926.5:p.Pro148=
NM_001001412.3:c.444T>A NP_001001412.3:p.Pro148=
NM_001001412.4:c.444T>A MANE Select NP_001001412.3:p.Pro148=
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Search 100 bp 3'