Canonical Allele Identifier: CA393088730
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1480609
ClinVar RCV Id: RCV002000332
dbSNP Id: rs2151214653
gnomAD v4: 15-73323569-G-A
MyVariant Identifiers: chr15:g.73615910G>A (hg19) chr15:g.73323569G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323569G>A , CM000677.2:g.73323569G>A GRCh38
NC_000015.9:g.73615910G>A , CM000677.1:g.73615910G>A GRCh37
NC_000015.8:g.71402963G>A NCBI36
NG_009063.1:g.50696C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.2524C>T MANE Select ENSP00000261917.3:p.Pro842Ser
ENST00000261917.3:c.2524C>T ENSP00000261917.3:p.Pro842Ser
NM_005477.2:c.2524C>T NP_005468.1:p.Pro842Ser
XM_011521148.1:c.1306C>T XP_011519450.1:p.Pro436Ser
XM_011521148.2:c.1306C>T XP_011519450.1:p.Pro436Ser
NM_005477.3:c.2524C>T MANE Select NP_005468.1:p.Pro842Ser
Search 100 bp 5'
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