Canonical Allele Identifier: CA393097385
Gene: HCN4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.73659971A>C (hg19) chr15:g.73367630A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367630A>C , CM000677.2:g.73367630A>C GRCh38
NC_000015.9:g.73659971A>C , CM000677.1:g.73659971A>C GRCh37
NC_000015.8:g.71447024A>C NCBI36
NG_009063.1:g.6635T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.641T>G MANE Select ENSP00000261917.3:p.Met214Arg
ENST00000261917.3:c.641T>G ENSP00000261917.3:p.Met214Arg
NM_005477.2:c.641T>G NP_005468.1:p.Met214Arg
NM_005477.3:c.641T>G MANE Select NP_005468.1:p.Met214Arg
Search 100 bp 5'
Search 100 bp 3'