Canonical Allele Identifier: CA2187188753
Gene: HCN4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323885G= , CM000677.2:g.73323885G= GRCh38
NC_000015.9:g.73616226G= , CM000677.1:g.73616226G= GRCh37
NC_000015.8:g.71403279G= NCBI36
NG_009063.1:g.50380C=

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.2208C= MANE Select ENSP00000261917.3:p.Tyr736=
ENST00000261917.3:c.2208C= ENSP00000261917.3:p.Tyr736=
NM_005477.2:c.2208C= NP_005468.1:p.Tyr736=
XM_011521148.1:c.990C= XP_011519450.1:p.Tyr330=
XM_011521148.2:c.990C= XP_011519450.1:p.Tyr330=
NM_005477.3:c.2208C= MANE Select NP_005468.1:p.Tyr736=