Canonical Allele Identifier: CA393097386
Gene: HCN4 HGNC NCBI

Linked Data

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

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

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.641T>C MANE Select ENSP00000261917.3:p.Met214Thr
ENST00000261917.3:c.641T>C ENSP00000261917.3:p.Met214Thr
NM_005477.2:c.641T>C NP_005468.1:p.Met214Thr
NM_005477.3:c.641T>C MANE Select NP_005468.1:p.Met214Thr
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