Canonical Allele Identifier: CA393088230
Gene: HCN4 HGNC NCBI

Linked Data

gnomAD v4: 15-73323358-T-A
COSMIC: COSM5849727
MyVariant Identifiers: chr15:g.73615699T>A (hg19) chr15:g.73323358T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323358T>A , CM000677.2:g.73323358T>A GRCh38
NC_000015.9:g.73615699T>A , CM000677.1:g.73615699T>A GRCh37
NC_000015.8:g.71402752T>A NCBI36
NG_009063.1:g.50907A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.2735A>T MANE Select ENSP00000261917.3:p.Lys912Met
ENST00000261917.3:c.2735A>T ENSP00000261917.3:p.Lys912Met
NM_005477.2:c.2735A>T NP_005468.1:p.Lys912Met
XM_011521148.1:c.1517A>T XP_011519450.1:p.Lys506Met
XM_011521148.2:c.1517A>T XP_011519450.1:p.Lys506Met
NM_005477.3:c.2735A>T MANE Select NP_005468.1:p.Lys912Met
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