Canonical Allele Identifier: CA393098477

Gene: HCN4

Linked Data

• dbSNP Id: rs1287771387
• gnomAD v2: 15-73660324-G-C
• gnomAD v4: 15-73367983-G-C
• MyVariant Identifiers: chr15:g.73660324G>C (hg19) ; chr15:g.73367983G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73367983G>C , CM000677.2:g.73367983G>C	GRCh38
NC_000015.9:g.73660324G>C , CM000677.1:g.73660324G>C	GRCh37
NC_000015.8:g.71447377G>C	NCBI36
NG_009063.1:g.6282C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.288C>G MANE Select	ENSP00000261917.3:p.Phe96Leu
ENST00000261917.3:c.288C>G	ENSP00000261917.3:p.Phe96Leu
NM_005477.2:c.288C>G	NP_005468.1:p.Phe96Leu
NM_005477.3:c.288C>G MANE Select	NP_005468.1:p.Phe96Leu