Canonical Allele Identifier: CA7649056

Gene: HCN4

Linked Data

• ClinVar Variation Id: 404137
• ClinVar RCV Id: RCV000469737
• dbSNP Id: rs750833108
• ExAC: 15:73616140 G / C
• gnomAD v2: 15-73616140-G-C
• gnomAD v3: 15-73323799-G-C
• gnomAD v4: 15-73323799-G-C
• MyVariant Identifiers: chr15:g.73616140G>C (hg19) ; chr15:g.73323799G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73323799G>C , CM000677.2:g.73323799G>C	GRCh38
NC_000015.9:g.73616140G>C , CM000677.1:g.73616140G>C	GRCh37
NC_000015.8:g.71403193G>C	NCBI36
NG_009063.1:g.50466C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000261917.4:c.2294C>G MANE Select	ENSP00000261917.3:p.Ala765Gly
ENST00000261917.3:c.2294C>G	ENSP00000261917.3:p.Ala765Gly
NM_005477.2:c.2294C>G	NP_005468.1:p.Ala765Gly
XM_011521148.1:c.1076C>G	XP_011519450.1:p.Ala359Gly
XM_011521148.2:c.1076C>G	XP_011519450.1:p.Ala359Gly
NM_005477.3:c.2294C>G MANE Select	NP_005468.1:p.Ala765Gly