Canonical Allele Identifier: CA393085292
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs1398249882
MyVariant Identifiers: chr15:g.73614991T>C (hg19) chr15:g.73322650T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322650T>C , CM000677.2:g.73322650T>C GRCh38
NC_000015.9:g.73614991T>C , CM000677.1:g.73614991T>C GRCh37
NC_000015.8:g.71402044T>C NCBI36
NG_009063.1:g.51615A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3443A>G MANE Select ENSP00000261917.3:p.Gln1148Arg
ENST00000261917.3:c.3443A>G ENSP00000261917.3:p.Gln1148Arg
NM_005477.2:c.3443A>G NP_005468.1:p.Gln1148Arg
XM_011521148.1:c.2225A>G XP_011519450.1:p.Gln742Arg
XM_011521148.2:c.2225A>G XP_011519450.1:p.Gln742Arg
NM_005477.3:c.3443A>G MANE Select NP_005468.1:p.Gln1148Arg
Search 100 bp 5'
Search 100 bp 3'