Canonical Allele Identifier: CA491478112
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs1435673888
gnomAD v2: 15-73615344-G-A
gnomAD v4: 15-73323003-G-A
MyVariant Identifiers: chr15:g.73615344G>A (hg19) chr15:g.73323003G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323003G>A , CM000677.2:g.73323003G>A GRCh38
NC_000015.9:g.73615344G>A , CM000677.1:g.73615344G>A GRCh37
NC_000015.8:g.71402397G>A NCBI36
NG_009063.1:g.51262C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3090C>T MANE Select ENSP00000261917.3:p.His1030=
ENST00000261917.3:c.3090C>T ENSP00000261917.3:p.His1030=
NM_005477.2:c.3090C>T NP_005468.1:p.His1030=
XM_011521148.1:c.1872C>T XP_011519450.1:p.His624=
XM_011521148.2:c.1872C>T XP_011519450.1:p.His624=
NM_005477.3:c.3090C>T MANE Select NP_005468.1:p.His1030=
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