Canonical Allele Identifier: CA7648925
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1003330
ClinVar RCV Id: RCV001299867
dbSNP Id: rs200495478
ExAC: 15:73615517 C / A
gnomAD v2: 15-73615517-C-A
gnomAD v3: 15-73323176-C-A
gnomAD v4: 15-73323176-C-A
MyVariant Identifiers: chr15:g.73615517C>A (hg19) chr15:g.73323176C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323176C>A , CM000677.2:g.73323176C>A GRCh38
NC_000015.9:g.73615517C>A , CM000677.1:g.73615517C>A GRCh37
NC_000015.8:g.71402570C>A NCBI36
NG_009063.1:g.51089G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.2917G>T MANE Select ENSP00000261917.3:p.Gly973Trp
ENST00000261917.3:c.2917G>T ENSP00000261917.3:p.Gly973Trp
NM_005477.2:c.2917G>T NP_005468.1:p.Gly973Trp
XM_011521148.1:c.1699G>T XP_011519450.1:p.Gly567Trp
XM_011521148.2:c.1699G>T XP_011519450.1:p.Gly567Trp
NM_005477.3:c.2917G>T MANE Select NP_005468.1:p.Gly973Trp
Search 100 bp 5'
Search 100 bp 3'