Canonical Allele Identifier: CA393085413
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322699T>C , CM000677.2:g.73322699T>C GRCh38
NC_000015.9:g.73615040T>C , CM000677.1:g.73615040T>C GRCh37
NC_000015.8:g.71402093T>C NCBI36
NG_009063.1:g.51566A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3394A>G MANE Select ENSP00000261917.3:p.Ser1132Gly
ENST00000261917.3:c.3394A>G ENSP00000261917.3:p.Ser1132Gly
NM_005477.2:c.3394A>G NP_005468.1:p.Ser1132Gly
XM_011521148.1:c.2176A>G XP_011519450.1:p.Ser726Gly
XM_011521148.2:c.2176A>G XP_011519450.1:p.Ser726Gly
NM_005477.3:c.3394A>G MANE Select NP_005468.1:p.Ser1132Gly