Canonical Allele Identifier: CA393098104
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1737905
ClinVar RCV Id: RCV002323395
dbSNP Id: rs2043136336
gnomAD v4: 15-73367861-G-A
MyVariant Identifiers: chr15:g.73660202G>A (hg19) chr15:g.73367861G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367861G>A , CM000677.2:g.73367861G>A GRCh38
NC_000015.9:g.73660202G>A , CM000677.1:g.73660202G>A GRCh37
NC_000015.8:g.71447255G>A NCBI36
NG_009063.1:g.6404C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.410C>T MANE Select ENSP00000261917.3:p.Ala137Val
ENST00000261917.3:c.410C>T ENSP00000261917.3:p.Ala137Val
NM_005477.2:c.410C>T NP_005468.1:p.Ala137Val
NM_005477.3:c.410C>T MANE Select NP_005468.1:p.Ala137Val
Search 100 bp 5'
Search 100 bp 3'