Canonical Allele Identifier: CA393097922

Gene: HCN4

Linked Data

• MyVariant Identifiers: chr15:g.73660140A>C (hg19) ; chr15:g.73367799A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73367799A>C , CM000677.2:g.73367799A>C	GRCh38
NC_000015.9:g.73660140A>C , CM000677.1:g.73660140A>C	GRCh37
NC_000015.8:g.71447193A>C	NCBI36
NG_009063.1:g.6466T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.472T>G MANE Select	ENSP00000261917.3:p.Ser158Ala
ENST00000261917.3:c.472T>G	ENSP00000261917.3:p.Ser158Ala
NM_005477.2:c.472T>G	NP_005468.1:p.Ser158Ala
NM_005477.3:c.472T>G MANE Select	NP_005468.1:p.Ser158Ala