Canonical Allele Identifier: CA393086091

Gene: HCN4

Linked Data

• gnomAD v4: 15-73322930-G-T
• MyVariant Identifiers: chr15:g.73615271G>T (hg19) ; chr15:g.73322930G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73322930G>T , CM000677.2:g.73322930G>T	GRCh38
NC_000015.9:g.73615271G>T , CM000677.1:g.73615271G>T	GRCh37
NC_000015.8:g.71402324G>T	NCBI36
NG_009063.1:g.51335C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.3163C>A MANE Select	ENSP00000261917.3:p.Pro1055Thr
ENST00000261917.3:c.3163C>A	ENSP00000261917.3:p.Pro1055Thr
NM_005477.2:c.3163C>A	NP_005468.1:p.Pro1055Thr
XM_011521148.1:c.1945C>A	XP_011519450.1:p.Pro649Thr
XM_011521148.2:c.1945C>A	XP_011519450.1:p.Pro649Thr
NM_005477.3:c.3163C>A MANE Select	NP_005468.1:p.Pro1055Thr