Canonical Allele Identifier: CA393086022
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs1255115138
gnomAD v3: 15-73322893-T-G
gnomAD v4: 15-73322893-T-G
MyVariant Identifiers: chr15:g.73615234T>G (hg19) chr15:g.73322893T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322893T>G , CM000677.2:g.73322893T>G GRCh38
NC_000015.9:g.73615234T>G , CM000677.1:g.73615234T>G GRCh37
NC_000015.8:g.71402287T>G NCBI36
NG_009063.1:g.51372A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3200A>C MANE Select ENSP00000261917.3:p.Gln1067Pro
ENST00000261917.3:c.3200A>C ENSP00000261917.3:p.Gln1067Pro
NM_005477.2:c.3200A>C NP_005468.1:p.Gln1067Pro
XM_011521148.1:c.1982A>C XP_011519450.1:p.Gln661Pro
XM_011521148.2:c.1982A>C XP_011519450.1:p.Gln661Pro
NM_005477.3:c.3200A>C MANE Select NP_005468.1:p.Gln1067Pro
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