Canonical Allele Identifier: CA393098077

Gene: HCN4

Linked Data

• MyVariant Identifiers: chr15:g.73660191C>G (hg19) ; chr15:g.73367850C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73367850C>G , CM000677.2:g.73367850C>G	GRCh38
NC_000015.9:g.73660191C>G , CM000677.1:g.73660191C>G	GRCh37
NC_000015.8:g.71447244C>G	NCBI36
NG_009063.1:g.6415G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.421G>C MANE Select	ENSP00000261917.3:p.Glu141Gln
ENST00000261917.3:c.421G>C	ENSP00000261917.3:p.Glu141Gln
NM_005477.2:c.421G>C	NP_005468.1:p.Glu141Gln
NM_005477.3:c.421G>C MANE Select	NP_005468.1:p.Glu141Gln