Canonical Allele Identifier: CA491479319
Gene: HCN4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.73660225C>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367884C>G , CM000677.2:g.73367884C>G GRCh38
NC_000015.9:g.73660225C>G , CM000677.1:g.73660225C>G GRCh37
NC_000015.8:g.71447278C>G NCBI36
NG_009063.1:g.6381G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.387G>C MANE Select ENSP00000261917.3:p.Arg129=
ENST00000261917.3:c.387G>C ENSP00000261917.3:p.Arg129=
NM_005477.2:c.387G>C NP_005468.1:p.Arg129=
NM_005477.3:c.387G>C MANE Select NP_005468.1:p.Arg129=
Search 100 bp 5'
Search 100 bp 3'