Canonical Allele Identifier: CA272700354
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2880101
ClinVar RCV Id: RCV003615079
dbSNP Id: rs1044205586
gnomAD v4: 15-73367851-G-T
MyVariant Identifiers: chr15:g.73660192G>T (hg19) chr15:g.73367851G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367851G>T , CM000677.2:g.73367851G>T GRCh38
NC_000015.9:g.73660192G>T , CM000677.1:g.73660192G>T GRCh37
NC_000015.8:g.71447245G>T NCBI36
NG_009063.1:g.6414C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.420C>A MANE Select ENSP00000261917.3:p.Gly140=
ENST00000261917.3:c.420C>A ENSP00000261917.3:p.Gly140=
NM_005477.2:c.420C>A NP_005468.1:p.Gly140=
NM_005477.3:c.420C>A MANE Select NP_005468.1:p.Gly140=
Search 100 bp 5'
Search 100 bp 3'