Canonical Allele Identifier: CA491478523

Gene: HCN4

Linked Data

• gnomAD v4: 15-73323708-G-T
• MyVariant Identifiers: chr15:g.73616049G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73323708G>T , CM000677.2:g.73323708G>T	GRCh38
NC_000015.9:g.73616049G>T , CM000677.1:g.73616049G>T	GRCh37
NC_000015.8:g.71403102G>T	NCBI36
NG_009063.1:g.50557C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000261917.4:c.2385C>A MANE Select	ENSP00000261917.3:p.Leu795=
ENST00000261917.3:c.2385C>A	ENSP00000261917.3:p.Leu795=
NM_005477.2:c.2385C>A	NP_005468.1:p.Leu795=
XM_011521148.1:c.1167C>A	XP_011519450.1:p.Leu389=
XM_011521148.2:c.1167C>A	XP_011519450.1:p.Leu389=
NM_005477.3:c.2385C>A MANE Select	NP_005468.1:p.Leu795=