Canonical Allele Identifier: CA393086776
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs1395656450
gnomAD v2: 15-73615493-C-T
gnomAD v4: 15-73323152-C-T
MyVariant Identifiers: chr15:g.73615493C>T (hg19) chr15:g.73323152C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323152C>T , CM000677.2:g.73323152C>T GRCh38
NC_000015.9:g.73615493C>T , CM000677.1:g.73615493C>T GRCh37
NC_000015.8:g.71402546C>T NCBI36
NG_009063.1:g.51113G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.2941G>A MANE Select ENSP00000261917.3:p.Glu981Lys
ENST00000261917.3:c.2941G>A ENSP00000261917.3:p.Glu981Lys
NM_005477.2:c.2941G>A NP_005468.1:p.Glu981Lys
XM_011521148.1:c.1723G>A XP_011519450.1:p.Glu575Lys
XM_011521148.2:c.1723G>A XP_011519450.1:p.Glu575Lys
NM_005477.3:c.2941G>A MANE Select NP_005468.1:p.Glu981Lys
Search 100 bp 5'
Search 100 bp 3'