Canonical Allele Identifier: CA393097205
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs1351390854

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367573A>G , CM000677.2:g.73367573A>G GRCh38
NC_000015.9:g.73659914A>G , CM000677.1:g.73659914A>G GRCh37
NC_000015.8:g.71446967A>G NCBI36
NG_009063.1:g.6692T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.698T>C MANE Select ENSP00000261917.3:p.Met233Thr
ENST00000261917.3:c.698T>C ENSP00000261917.3:p.Met233Thr
NM_005477.2:c.698T>C NP_005468.1:p.Met233Thr
NM_005477.3:c.698T>C MANE Select NP_005468.1:p.Met233Thr