Canonical Allele Identifier: CA393098067

Gene: HCN4

Linked Data

• gnomAD v4: 15-73367847-C-G
• MyVariant Identifiers: chr15:g.73660188C>G (hg19) ; chr15:g.73367847C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73367847C>G , CM000677.2:g.73367847C>G	GRCh38
NC_000015.9:g.73660188C>G , CM000677.1:g.73660188C>G	GRCh37
NC_000015.8:g.71447241C>G	NCBI36
NG_009063.1:g.6418G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.424G>C MANE Select	ENSP00000261917.3:p.Asp142His
ENST00000261917.3:c.424G>C	ENSP00000261917.3:p.Asp142His
NM_005477.2:c.424G>C	NP_005468.1:p.Asp142His
NM_005477.3:c.424G>C MANE Select	NP_005468.1:p.Asp142His