Canonical Allele Identifier: CA7649479
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs760442925

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367899G>C , CM000677.2:g.73367899G>C GRCh38
NC_000015.9:g.73660240G>C , CM000677.1:g.73660240G>C GRCh37
NC_000015.8:g.71447293G>C NCBI36
NG_009063.1:g.6366C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.372C>G MANE Select ENSP00000261917.3:p.Asp124Glu
ENST00000261917.3:c.372C>G ENSP00000261917.3:p.Asp124Glu
NM_005477.2:c.372C>G NP_005468.1:p.Asp124Glu
NM_005477.3:c.372C>G MANE Select NP_005468.1:p.Asp124Glu