Canonical Allele Identifier: CA393099098
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73368191T>C , CM000677.2:g.73368191T>C GRCh38
NC_000015.9:g.73660532T>C , CM000677.1:g.73660532T>C GRCh37
NC_000015.8:g.71447585T>C NCBI36
NG_009063.1:g.6074A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.80A>G MANE Select ENSP00000261917.3:p.Asp27Gly
ENST00000261917.3:c.80A>G ENSP00000261917.3:p.Asp27Gly
NM_005477.2:c.80A>G NP_005468.1:p.Asp27Gly
NM_005477.3:c.80A>G MANE Select NP_005468.1:p.Asp27Gly