Canonical Allele Identifier: CA393088381
Gene: HCN4 HGNC NCBI

Linked Data

gnomAD v4: 15-73323398-C-A
MyVariant Identifiers: chr15:g.73615739C>A (hg19) chr15:g.73323398C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323398C>A , CM000677.2:g.73323398C>A GRCh38
NC_000015.9:g.73615739C>A , CM000677.1:g.73615739C>A GRCh37
NC_000015.8:g.71402792C>A NCBI36
NG_009063.1:g.50867G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.2695G>T MANE Select ENSP00000261917.3:p.Val899Leu
ENST00000261917.3:c.2695G>T ENSP00000261917.3:p.Val899Leu
NM_005477.2:c.2695G>T NP_005468.1:p.Val899Leu
XM_011521148.1:c.1477G>T XP_011519450.1:p.Val493Leu
XM_011521148.2:c.1477G>T XP_011519450.1:p.Val493Leu
NM_005477.3:c.2695G>T MANE Select NP_005468.1:p.Val899Leu
Search 100 bp 5'
Search 100 bp 3'