Canonical Allele Identifier: CA7648997
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs750310564
ExAC: 15:73615854 T / C
gnomAD v2: 15-73615854-T-C
gnomAD v3: 15-73323513-T-C
gnomAD v4: 15-73323513-T-C
MyVariant Identifiers: chr15:g.73615854T>C (hg19) chr15:g.73323513T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323513T>C , CM000677.2:g.73323513T>C GRCh38
NC_000015.9:g.73615854T>C , CM000677.1:g.73615854T>C GRCh37
NC_000015.8:g.71402907T>C NCBI36
NG_009063.1:g.50752A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.2580A>G MANE Select ENSP00000261917.3:p.Gln860=
ENST00000261917.3:c.2580A>G ENSP00000261917.3:p.Gln860=
NM_005477.2:c.2580A>G NP_005468.1:p.Gln860=
XM_011521148.1:c.1362A>G XP_011519450.1:p.Gln454=
XM_011521148.2:c.1362A>G XP_011519450.1:p.Gln454=
NM_005477.3:c.2580A>G MANE Select NP_005468.1:p.Gln860=
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