Canonical Allele Identifier: CA7648846
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs761260529
ExAC: 15:73615114 T / A
gnomAD v2: 15-73615114-T-A
MyVariant Identifiers: chr15:g.73615114T>A (hg19) chr15:g.73322773T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322773T>A , CM000677.2:g.73322773T>A GRCh38
NC_000015.9:g.73615114T>A , CM000677.1:g.73615114T>A GRCh37
NC_000015.8:g.71402167T>A NCBI36
NG_009063.1:g.51492A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.3320A>T MANE Select ENSP00000261917.3:p.His1107Leu
ENST00000261917.3:c.3320A>T ENSP00000261917.3:p.His1107Leu
NM_005477.2:c.3320A>T NP_005468.1:p.His1107Leu
XM_011521148.1:c.2102A>T XP_011519450.1:p.His701Leu
XM_011521148.2:c.2102A>T XP_011519450.1:p.His701Leu
NM_005477.3:c.3320A>T MANE Select NP_005468.1:p.His1107Leu
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