Canonical Allele Identifier: CA491478025
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1597291
ClinVar RCV Id: RCV002117685
dbSNP Id: rs2151214076
gnomAD v4: 15-73322949-G-A
MyVariant Identifiers: chr15:g.73615290G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322949G>A , CM000677.2:g.73322949G>A GRCh38
NC_000015.9:g.73615290G>A , CM000677.1:g.73615290G>A GRCh37
NC_000015.8:g.71402343G>A NCBI36
NG_009063.1:g.51316C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3144C>T MANE Select ENSP00000261917.3:p.Ser1048=
ENST00000261917.3:c.3144C>T ENSP00000261917.3:p.Ser1048=
NM_005477.2:c.3144C>T NP_005468.1:p.Ser1048=
XM_011521148.1:c.1926C>T XP_011519450.1:p.Ser642=
XM_011521148.2:c.1926C>T XP_011519450.1:p.Ser642=
NM_005477.3:c.3144C>T MANE Select NP_005468.1:p.Ser1048=
Search 100 bp 5'
Search 100 bp 3'