Canonical Allele Identifier: CA393085428
Gene: HCN4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.73615047A>C (hg19) chr15:g.73322706A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322706A>C , CM000677.2:g.73322706A>C GRCh38
NC_000015.9:g.73615047A>C , CM000677.1:g.73615047A>C GRCh37
NC_000015.8:g.71402100A>C NCBI36
NG_009063.1:g.51559T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3387T>G MANE Select ENSP00000261917.3:p.Ser1129Arg
ENST00000261917.3:c.3387T>G ENSP00000261917.3:p.Ser1129Arg
NM_005477.2:c.3387T>G NP_005468.1:p.Ser1129Arg
XM_011521148.1:c.2169T>G XP_011519450.1:p.Ser723Arg
XM_011521148.2:c.2169T>G XP_011519450.1:p.Ser723Arg
NM_005477.3:c.3387T>G MANE Select NP_005468.1:p.Ser1129Arg
Search 100 bp 5'
Search 100 bp 3'