Canonical Allele Identifier: CA393089452
Gene: HCN4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.73616236A>C (hg19) chr15:g.73323895A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323895A>C , CM000677.2:g.73323895A>C GRCh38
NC_000015.9:g.73616236A>C , CM000677.1:g.73616236A>C GRCh37
NC_000015.8:g.71403289A>C NCBI36
NG_009063.1:g.50370T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.2198T>G MANE Select ENSP00000261917.3:p.Val733Gly
ENST00000261917.3:c.2198T>G ENSP00000261917.3:p.Val733Gly
NM_005477.2:c.2198T>G NP_005468.1:p.Val733Gly
XM_011521148.1:c.980T>G XP_011519450.1:p.Val327Gly
XM_011521148.2:c.980T>G XP_011519450.1:p.Val327Gly
NM_005477.3:c.2198T>G MANE Select NP_005468.1:p.Val733Gly
Search 100 bp 5'
Search 100 bp 3'