Canonical Allele Identifier: CA393089449

Gene: HCN4

Linked Data

• MyVariant Identifiers: chr15:g.73616234A>G (hg19) ; chr15:g.73323893A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73323893A>G , CM000677.2:g.73323893A>G	GRCh38
NC_000015.9:g.73616234A>G , CM000677.1:g.73616234A>G	GRCh37
NC_000015.8:g.71403287A>G	NCBI36
NG_009063.1:g.50372T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000261917.4:c.2200T>C MANE Select	ENSP00000261917.3:p.Phe734Leu
ENST00000261917.3:c.2200T>C	ENSP00000261917.3:p.Phe734Leu
NM_005477.2:c.2200T>C	NP_005468.1:p.Phe734Leu
XM_011521148.1:c.982T>C	XP_011519450.1:p.Phe328Leu
XM_011521148.2:c.982T>C	XP_011519450.1:p.Phe328Leu
NM_005477.3:c.2200T>C MANE Select	NP_005468.1:p.Phe734Leu