Canonical Allele Identifier: CA272700126

Gene: HCN4

Linked Data

• dbSNP Id: rs971709325
• gnomAD v2: 15-73659992-C-T
• gnomAD v4: 15-73367651-C-T
• MyVariant Identifiers: chr15:g.73659992C>T (hg19) ; chr15:g.73367651C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73367651C>T , CM000677.2:g.73367651C>T	GRCh38
NC_000015.9:g.73659992C>T , CM000677.1:g.73659992C>T	GRCh37
NC_000015.8:g.71447045C>T	NCBI36
NG_009063.1:g.6614G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.620G>A MANE Select	ENSP00000261917.3:p.Arg207His
ENST00000261917.3:c.620G>A	ENSP00000261917.3:p.Arg207His
NM_005477.2:c.620G>A	NP_005468.1:p.Arg207His
NM_005477.3:c.620G>A MANE Select	NP_005468.1:p.Arg207His