Canonical Allele Identifier: CA393086131

Gene: HCN4

Linked Data

• gnomAD v4: 15-73322948-G-T
• MyVariant Identifiers: chr15:g.73615289G>T (hg19) ; chr15:g.73322948G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73322948G>T , CM000677.2:g.73322948G>T	GRCh38
NC_000015.9:g.73615289G>T , CM000677.1:g.73615289G>T	GRCh37
NC_000015.8:g.71402342G>T	NCBI36
NG_009063.1:g.51317C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.3145C>A MANE Select	ENSP00000261917.3:p.His1049Asn
ENST00000261917.3:c.3145C>A	ENSP00000261917.3:p.His1049Asn
NM_005477.2:c.3145C>A	NP_005468.1:p.His1049Asn
XM_011521148.1:c.1927C>A	XP_011519450.1:p.His643Asn
XM_011521148.2:c.1927C>A	XP_011519450.1:p.His643Asn
NM_005477.3:c.3145C>A MANE Select	NP_005468.1:p.His1049Asn