Canonical Allele Identifier: CA393086020

Gene: HCN4

Linked Data

• MyVariant Identifiers: chr15:g.73615234T>A (hg19) ; chr15:g.73322893T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73322893T>A , CM000677.2:g.73322893T>A	GRCh38
NC_000015.9:g.73615234T>A , CM000677.1:g.73615234T>A	GRCh37
NC_000015.8:g.71402287T>A	NCBI36
NG_009063.1:g.51372A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.3200A>T MANE Select	ENSP00000261917.3:p.Gln1067Leu
ENST00000261917.3:c.3200A>T	ENSP00000261917.3:p.Gln1067Leu
NM_005477.2:c.3200A>T	NP_005468.1:p.Gln1067Leu
XM_011521148.1:c.1982A>T	XP_011519450.1:p.Gln661Leu
XM_011521148.2:c.1982A>T	XP_011519450.1:p.Gln661Leu
NM_005477.3:c.3200A>T MANE Select	NP_005468.1:p.Gln1067Leu