Canonical Allele Identifier: CA471499622
Gene: CALHM1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.105218082G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.103458325G>A , CM000672.2:g.103458325G>A GRCh38
NC_000010.10:g.105218082G>A , CM000672.1:g.105218082G>A GRCh37
NC_000010.9:g.105208072G>A NCBI36
NG_016855.1:g.5567C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000329905.6:c.427C>T MANE Select ENSP00000329926.6:p.Leu143=
ENST00000329905.5:c.427C>T ENSP00000329926.5:p.Leu143=
NM_001001412.3:c.427C>T NP_001001412.3:p.Leu143=
NM_001001412.4:c.427C>T MANE Select NP_001001412.3:p.Leu143=
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