Canonical Allele Identifier: CA2187187647
Gene: HCN4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323179G= , CM000677.2:g.73323179G= GRCh38
NC_000015.9:g.73615520G= , CM000677.1:g.73615520G= GRCh37
NC_000015.8:g.71402573G= NCBI36
NG_009063.1:g.51086C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.2914C= MANE Select ENSP00000261917.3:p.Pro972=
ENST00000261917.3:c.2914C= ENSP00000261917.3:p.Pro972=
NM_005477.2:c.2914C= NP_005468.1:p.Pro972=
XM_011521148.1:c.1696C= XP_011519450.1:p.Pro566=
XM_011521148.2:c.1696C= XP_011519450.1:p.Pro566=
NM_005477.3:c.2914C= MANE Select NP_005468.1:p.Pro972=