Canonical Allele Identifier: CA393086272

Gene: HCN4

Linked Data

• MyVariant Identifiers: chr15:g.73615361G>C (hg19) ; chr15:g.73323020G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73323020G>C , CM000677.2:g.73323020G>C	GRCh38
NC_000015.9:g.73615361G>C , CM000677.1:g.73615361G>C	GRCh37
NC_000015.8:g.71402414G>C	NCBI36
NG_009063.1:g.51245C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.3073C>G MANE Select	ENSP00000261917.3:p.Leu1025Val
ENST00000261917.3:c.3073C>G	ENSP00000261917.3:p.Leu1025Val
NM_005477.2:c.3073C>G	NP_005468.1:p.Leu1025Val
XM_011521148.1:c.1855C>G	XP_011519450.1:p.Leu619Val
XM_011521148.2:c.1855C>G	XP_011519450.1:p.Leu619Val
NM_005477.3:c.3073C>G MANE Select	NP_005468.1:p.Leu1025Val