Canonical Allele Identifier: CA491151651
Gene: HCN4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.73622034G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73329693G>T , CM000677.2:g.73329693G>T GRCh38
NC_000015.9:g.73622034G>T , CM000677.1:g.73622034G>T GRCh37
NC_000015.8:g.71409087G>T NCBI36
NG_009063.1:g.44572C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.1470C>A MANE Select ENSP00000261917.3:p.Ser490=
ENST00000261917.3:c.1470C>A ENSP00000261917.3:p.Ser490=
NM_005477.2:c.1470C>A NP_005468.1:p.Ser490=
XM_011521148.1:c.252C>A XP_011519450.1:p.Ser84=
XM_011521148.2:c.252C>A XP_011519450.1:p.Ser84=
NM_005477.3:c.1470C>A MANE Select NP_005468.1:p.Ser490=