Canonical Allele Identifier: CA491478705
Gene: HCN4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.73616124C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323783C>G , CM000677.2:g.73323783C>G GRCh38
NC_000015.9:g.73616124C>G , CM000677.1:g.73616124C>G GRCh37
NC_000015.8:g.71403177C>G NCBI36
NG_009063.1:g.50482G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.2310G>C MANE Select ENSP00000261917.3:p.Thr770=
ENST00000261917.3:c.2310G>C ENSP00000261917.3:p.Thr770=
NM_005477.2:c.2310G>C NP_005468.1:p.Thr770=
XM_011521148.1:c.1092G>C XP_011519450.1:p.Thr364=
XM_011521148.2:c.1092G>C XP_011519450.1:p.Thr364=
NM_005477.3:c.2310G>C MANE Select NP_005468.1:p.Thr770=
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