Canonical Allele Identifier: CA393098199
Gene: HCN4 HGNC NCBI

Linked Data

gnomAD v4: 15-73367889-C-A
COSMIC: COSM1172279
MyVariant Identifiers: chr15:g.73660230C>A (hg19) chr15:g.73367889C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367889C>A , CM000677.2:g.73367889C>A GRCh38
NC_000015.9:g.73660230C>A , CM000677.1:g.73660230C>A GRCh37
NC_000015.8:g.71447283C>A NCBI36
NG_009063.1:g.6376G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.382G>T MANE Select ENSP00000261917.3:p.Glu128Ter
ENST00000261917.3:c.382G>T ENSP00000261917.3:p.Glu128Ter
NM_005477.2:c.382G>T NP_005468.1:p.Glu128Ter
NM_005477.3:c.382G>T MANE Select NP_005468.1:p.Glu128Ter
Search 100 bp 5'
Search 100 bp 3'