Canonical Allele Identifier: CA471499556
Gene: CALHM1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.105218170G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.103458413G>C , CM000672.2:g.103458413G>C GRCh38
NC_000010.10:g.105218170G>C , CM000672.1:g.105218170G>C GRCh37
NC_000010.9:g.105208160G>C NCBI36
NG_016855.1:g.5479C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000329905.6:c.339C>G MANE Select ENSP00000329926.6:p.Val113=
ENST00000329905.5:c.339C>G ENSP00000329926.5:p.Val113=
NM_001001412.3:c.339C>G NP_001001412.3:p.Val113=
NM_001001412.4:c.339C>G MANE Select NP_001001412.3:p.Val113=
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