Canonical Allele Identifier: CA7649084
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs761839180
ExAC: 15:73616278 G / T
gnomAD v2: 15-73616278-G-T
gnomAD v4: 15-73323937-G-T
MyVariant Identifiers: chr15:g.73616278G>T (hg19) chr15:g.73323937G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323937G>T , CM000677.2:g.73323937G>T GRCh38
NC_000015.9:g.73616278G>T , CM000677.1:g.73616278G>T GRCh37
NC_000015.8:g.71403331G>T NCBI36
NG_009063.1:g.50328C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.2156C>A MANE Select ENSP00000261917.3:p.Ser719Tyr
ENST00000261917.3:c.2156C>A ENSP00000261917.3:p.Ser719Tyr
NM_005477.2:c.2156C>A NP_005468.1:p.Ser719Tyr
XM_011521148.1:c.938C>A XP_011519450.1:p.Ser313Tyr
XM_011521148.2:c.938C>A XP_011519450.1:p.Ser313Tyr
NM_005477.3:c.2156C>A MANE Select NP_005468.1:p.Ser719Tyr
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