Canonical Allele Identifier: CA393093431
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73329599A>C , CM000677.2:g.73329599A>C GRCh38
NC_000015.9:g.73621940A>C , CM000677.1:g.73621940A>C GRCh37
NC_000015.8:g.71408993A>C NCBI36
NG_009063.1:g.44666T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.1564T>G MANE Select ENSP00000261917.3:p.Ser522Ala
ENST00000261917.3:c.1564T>G ENSP00000261917.3:p.Ser522Ala
NM_005477.2:c.1564T>G NP_005468.1:p.Ser522Ala
XM_011521148.1:c.346T>G XP_011519450.1:p.Ser116Ala
XM_011521148.2:c.346T>G XP_011519450.1:p.Ser116Ala
NM_005477.3:c.1564T>G MANE Select NP_005468.1:p.Ser522Ala