Canonical Allele Identifier: CA491479544
Gene: HCN4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.73660039C>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367698C>T , CM000677.2:g.73367698C>T GRCh38
NC_000015.9:g.73660039C>T , CM000677.1:g.73660039C>T GRCh37
NC_000015.8:g.71447092C>T NCBI36
NG_009063.1:g.6567G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.573G>A MANE Select ENSP00000261917.3:p.Glu191=
ENST00000261917.3:c.573G>A ENSP00000261917.3:p.Glu191=
NM_005477.2:c.573G>A NP_005468.1:p.Glu191=
NM_005477.3:c.573G>A MANE Select NP_005468.1:p.Glu191=
Search 100 bp 5'
Search 100 bp 3'