Canonical Allele Identifier: CA393088448
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs758929649
gnomAD v2: 15-73615765-G-T
gnomAD v4: 15-73323424-G-T
MyVariant Identifiers: chr15:g.73615765G>T (hg19) chr15:g.73323424G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323424G>T , CM000677.2:g.73323424G>T GRCh38
NC_000015.9:g.73615765G>T , CM000677.1:g.73615765G>T GRCh37
NC_000015.8:g.71402818G>T NCBI36
NG_009063.1:g.50841C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.2669C>A MANE Select ENSP00000261917.3:p.Pro890His
ENST00000261917.3:c.2669C>A ENSP00000261917.3:p.Pro890His
NM_005477.2:c.2669C>A NP_005468.1:p.Pro890His
XM_011521148.1:c.1451C>A XP_011519450.1:p.Pro484His
XM_011521148.2:c.1451C>A XP_011519450.1:p.Pro484His
NM_005477.3:c.2669C>A MANE Select NP_005468.1:p.Pro890His
Search 100 bp 5'
Search 100 bp 3'