Canonical Allele Identifier: CA393086677
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323136A>C , CM000677.2:g.73323136A>C GRCh38
NC_000015.9:g.73615477A>C , CM000677.1:g.73615477A>C GRCh37
NC_000015.8:g.71402530A>C NCBI36
NG_009063.1:g.51129T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.2957T>G MANE Select ENSP00000261917.3:p.Leu986Arg
ENST00000261917.3:c.2957T>G ENSP00000261917.3:p.Leu986Arg
NM_005477.2:c.2957T>G NP_005468.1:p.Leu986Arg
XM_011521148.1:c.1739T>G XP_011519450.1:p.Leu580Arg
XM_011521148.2:c.1739T>G XP_011519450.1:p.Leu580Arg
NM_005477.3:c.2957T>G MANE Select NP_005468.1:p.Leu986Arg