Canonical Allele Identifier: CA393085039
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322576T>G , CM000677.2:g.73322576T>G GRCh38
NC_000015.9:g.73614917T>G , CM000677.1:g.73614917T>G GRCh37
NC_000015.8:g.71401970T>G NCBI36
NG_009063.1:g.51689A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3517A>C MANE Select ENSP00000261917.3:p.Thr1173Pro
ENST00000261917.3:c.3517A>C ENSP00000261917.3:p.Thr1173Pro
NM_005477.2:c.3517A>C NP_005468.1:p.Thr1173Pro
XM_011521148.1:c.2299A>C XP_011519450.1:p.Thr767Pro
XM_011521148.2:c.2299A>C XP_011519450.1:p.Thr767Pro
NM_005477.3:c.3517A>C MANE Select NP_005468.1:p.Thr1173Pro