Canonical Allele Identifier: CA393086326
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323041C>T , CM000677.2:g.73323041C>T GRCh38
NC_000015.9:g.73615382C>T , CM000677.1:g.73615382C>T GRCh37
NC_000015.8:g.71402435C>T NCBI36
NG_009063.1:g.51224G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3052G>A MANE Select ENSP00000261917.3:p.Gly1018Ser
ENST00000261917.3:c.3052G>A ENSP00000261917.3:p.Gly1018Ser
NM_005477.2:c.3052G>A NP_005468.1:p.Gly1018Ser
XM_011521148.1:c.1834G>A XP_011519450.1:p.Gly612Ser
XM_011521148.2:c.1834G>A XP_011519450.1:p.Gly612Ser
NM_005477.3:c.3052G>A MANE Select NP_005468.1:p.Gly1018Ser