Canonical Allele Identifier: CA393085699
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322789G>T , CM000677.2:g.73322789G>T GRCh38
NC_000015.9:g.73615130G>T , CM000677.1:g.73615130G>T GRCh37
NC_000015.8:g.71402183G>T NCBI36
NG_009063.1:g.51476C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3304C>A MANE Select ENSP00000261917.3:p.Arg1102Ser
ENST00000261917.3:c.3304C>A ENSP00000261917.3:p.Arg1102Ser
NM_005477.2:c.3304C>A NP_005468.1:p.Arg1102Ser
XM_011521148.1:c.2086C>A XP_011519450.1:p.Arg696Ser
XM_011521148.2:c.2086C>A XP_011519450.1:p.Arg696Ser
NM_005477.3:c.3304C>A MANE Select NP_005468.1:p.Arg1102Ser