Canonical Allele Identifier: CA393098978

Gene: HCN4

Linked Data

• dbSNP Id: rs1300096638
• gnomAD v2: 15-73660494-G-A
• gnomAD v4: 15-73368153-G-A
• MyVariant Identifiers: chr15:g.73660494G>A (hg19) ; chr15:g.73368153G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73368153G>A , CM000677.2:g.73368153G>A	GRCh38
NC_000015.9:g.73660494G>A , CM000677.1:g.73660494G>A	GRCh37
NC_000015.8:g.71447547G>A	NCBI36
NG_009063.1:g.6112C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.118C>T MANE Select	ENSP00000261917.3:p.Arg40Cys
ENST00000261917.3:c.118C>T	ENSP00000261917.3:p.Arg40Cys
NM_005477.2:c.118C>T	NP_005468.1:p.Arg40Cys
NM_005477.3:c.118C>T MANE Select	NP_005468.1:p.Arg40Cys