Canonical Allele Identifier: CA16607135

Gene: HCN4

Linked Data

• ClinVar Variation Id: 383673
• ClinVar RCV Id: RCV000422785 ; RCV000945959
• dbSNP Id: rs947950341
• gnomAD v3: 15-73322625-T-C
• gnomAD v4: 15-73322625-T-C
• MyVariant Identifiers: chr15:g.73614966T>C (hg19) ; chr15:g.73322625T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73322625T>C , CM000677.2:g.73322625T>C	GRCh38
NC_000015.9:g.73614966T>C , CM000677.1:g.73614966T>C	GRCh37
NC_000015.8:g.71402019T>C	NCBI36
NG_009063.1:g.51640A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000261917.4:c.3468A>G MANE Select	ENSP00000261917.3:p.Thr1156=
ENST00000261917.3:c.3468A>G	ENSP00000261917.3:p.Thr1156=
NM_005477.2:c.3468A>G	NP_005468.1:p.Thr1156=
XM_011521148.1:c.2250A>G	XP_011519450.1:p.Thr750=
XM_011521148.2:c.2250A>G	XP_011519450.1:p.Thr750=
NM_005477.3:c.3468A>G MANE Select	NP_005468.1:p.Thr1156=