Canonical Allele Identifier: CA393094267
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73332147G>T , CM000677.2:g.73332147G>T GRCh38
NC_000015.9:g.73624488G>T , CM000677.1:g.73624488G>T GRCh37
NC_000015.8:g.71411541G>T NCBI36
NG_009063.1:g.42118C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.1355C>A MANE Select ENSP00000261917.3:p.Ser452Tyr
ENST00000261917.3:c.1355C>A ENSP00000261917.3:p.Ser452Tyr
NM_005477.2:c.1355C>A NP_005468.1:p.Ser452Tyr
XM_011521148.1:c.137C>A XP_011519450.1:p.Ser46Tyr
XM_011521148.2:c.137C>A XP_011519450.1:p.Ser46Tyr
NM_005477.3:c.1355C>A MANE Select NP_005468.1:p.Ser452Tyr