Canonical Allele Identifier: CA393098158
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367876A>C , CM000677.2:g.73367876A>C GRCh38
NC_000015.9:g.73660217A>C , CM000677.1:g.73660217A>C GRCh37
NC_000015.8:g.71447270A>C NCBI36
NG_009063.1:g.6389T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.395T>G MANE Select ENSP00000261917.3:p.Ile132Ser
ENST00000261917.3:c.395T>G ENSP00000261917.3:p.Ile132Ser
NM_005477.2:c.395T>G NP_005468.1:p.Ile132Ser
NM_005477.3:c.395T>G MANE Select NP_005468.1:p.Ile132Ser