Canonical Allele Identifier: CA491478347
Gene: HCN4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.73616133T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323792T>C , CM000677.2:g.73323792T>C GRCh38
NC_000015.9:g.73616133T>C , CM000677.1:g.73616133T>C GRCh37
NC_000015.8:g.71403186T>C NCBI36
NG_009063.1:g.50473A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.2301A>G MANE Select ENSP00000261917.3:p.Pro767=
ENST00000261917.3:c.2301A>G ENSP00000261917.3:p.Pro767=
NM_005477.2:c.2301A>G NP_005468.1:p.Pro767=
XM_011521148.1:c.1083A>G XP_011519450.1:p.Pro361=
XM_011521148.2:c.1083A>G XP_011519450.1:p.Pro361=
NM_005477.3:c.2301A>G MANE Select NP_005468.1:p.Pro767=
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