Canonical Allele Identifier: CA393088195
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs1595819830
gnomAD v4: 15-73323347-C-T
MyVariant Identifiers: chr15:g.73615688C>T (hg19) chr15:g.73323347C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323347C>T , CM000677.2:g.73323347C>T GRCh38
NC_000015.9:g.73615688C>T , CM000677.1:g.73615688C>T GRCh37
NC_000015.8:g.71402741C>T NCBI36
NG_009063.1:g.50918G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.2746G>A MANE Select ENSP00000261917.3:p.Gly916Ser
ENST00000261917.3:c.2746G>A ENSP00000261917.3:p.Gly916Ser
NM_005477.2:c.2746G>A NP_005468.1:p.Gly916Ser
XM_011521148.1:c.1528G>A XP_011519450.1:p.Gly510Ser
XM_011521148.2:c.1528G>A XP_011519450.1:p.Gly510Ser
NM_005477.3:c.2746G>A MANE Select NP_005468.1:p.Gly916Ser
Search 100 bp 5'
Search 100 bp 3'