Canonical Allele Identifier: CA393086250

Gene: HCN4

Linked Data

• gnomAD v4: 15-73323008-C-A
• MyVariant Identifiers: chr15:g.73615349C>A (hg19) ; chr15:g.73323008C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73323008C>A , CM000677.2:g.73323008C>A	GRCh38
NC_000015.9:g.73615349C>A , CM000677.1:g.73615349C>A	GRCh37
NC_000015.8:g.71402402C>A	NCBI36
NG_009063.1:g.51257G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.3085G>T MANE Select	ENSP00000261917.3:p.Gly1029Cys
ENST00000261917.3:c.3085G>T	ENSP00000261917.3:p.Gly1029Cys
NM_005477.2:c.3085G>T	NP_005468.1:p.Gly1029Cys
XM_011521148.1:c.1867G>T	XP_011519450.1:p.Gly623Cys
XM_011521148.2:c.1867G>T	XP_011519450.1:p.Gly623Cys
NM_005477.3:c.3085G>T MANE Select	NP_005468.1:p.Gly1029Cys