Canonical Allele Identifier: CA393085388
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322686C>G , CM000677.2:g.73322686C>G GRCh38
NC_000015.9:g.73615027C>G , CM000677.1:g.73615027C>G GRCh37
NC_000015.8:g.71402080C>G NCBI36
NG_009063.1:g.51579G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.3407G>C MANE Select ENSP00000261917.3:p.Gly1136Ala
ENST00000261917.3:c.3407G>C ENSP00000261917.3:p.Gly1136Ala
NM_005477.2:c.3407G>C NP_005468.1:p.Gly1136Ala
XM_011521148.1:c.2189G>C XP_011519450.1:p.Gly730Ala
XM_011521148.2:c.2189G>C XP_011519450.1:p.Gly730Ala
NM_005477.3:c.3407G>C MANE Select NP_005468.1:p.Gly1136Ala