Canonical Allele Identifier: CA393094325
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1349052
ClinVar RCV Id: RCV002050969 RCV002386593 RCV003388055
dbSNP Id: rs1444329166
gnomAD v3: 15-73332171-T-A
gnomAD v4: 15-73332171-T-A
MyVariant Identifiers: chr15:g.73624512T>A (hg19) chr15:g.73332171T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73332171T>A , CM000677.2:g.73332171T>A GRCh38
NC_000015.9:g.73624512T>A , CM000677.1:g.73624512T>A GRCh37
NC_000015.8:g.71411565T>A NCBI36
NG_009063.1:g.42094A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.1331A>T MANE Select ENSP00000261917.3:p.Asp444Val
ENST00000261917.3:c.1331A>T ENSP00000261917.3:p.Asp444Val
NM_005477.2:c.1331A>T NP_005468.1:p.Asp444Val
XM_011521148.1:c.113A>T XP_011519450.1:p.Asp38Val
XM_011521148.2:c.113A>T XP_011519450.1:p.Asp38Val
NM_005477.3:c.1331A>T MANE Select NP_005468.1:p.Asp444Val
Search 100 bp 5'
Search 100 bp 3'