Canonical Allele Identifier: CA7648930

Gene: HCN4

Linked Data

• ClinVar Variation Id: 392636
• ClinVar RCV Id: RCV000433991 ; RCV001323315
• dbSNP Id: rs548194804
• ExAC: 15:73615531 G / A
• gnomAD v2: 15-73615531-G-A
• gnomAD v3: 15-73323190-G-A
• gnomAD v4: 15-73323190-G-A
• MyVariant Identifiers: chr15:g.73615531G>A (hg19) ; chr15:g.73323190G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73323190G>A , CM000677.2:g.73323190G>A	GRCh38
NC_000015.9:g.73615531G>A , CM000677.1:g.73615531G>A	GRCh37
NC_000015.8:g.71402584G>A	NCBI36
NG_009063.1:g.51075C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.2903C>T MANE Select	ENSP00000261917.3:p.Pro968Leu
ENST00000261917.3:c.2903C>T	ENSP00000261917.3:p.Pro968Leu
NM_005477.2:c.2903C>T	NP_005468.1:p.Pro968Leu
XM_011521148.1:c.1685C>T	XP_011519450.1:p.Pro562Leu
XM_011521148.2:c.1685C>T	XP_011519450.1:p.Pro562Leu
NM_005477.3:c.2903C>T MANE Select	NP_005468.1:p.Pro968Leu