Canonical Allele Identifier: CA393097877

Gene: HCN4

Linked Data

• MyVariant Identifiers: chr15:g.73660127G>C (hg19) ; chr15:g.73367786G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73367786G>C , CM000677.2:g.73367786G>C	GRCh38
NC_000015.9:g.73660127G>C , CM000677.1:g.73660127G>C	GRCh37
NC_000015.8:g.71447180G>C	NCBI36
NG_009063.1:g.6479C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.485C>G MANE Select	ENSP00000261917.3:p.Ala162Gly
ENST00000261917.3:c.485C>G	ENSP00000261917.3:p.Ala162Gly
NM_005477.2:c.485C>G	NP_005468.1:p.Ala162Gly
NM_005477.3:c.485C>G MANE Select	NP_005468.1:p.Ala162Gly