Canonical Allele Identifier: CA393089147
Gene: HCN4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.73616126T>C (hg19) chr15:g.73323785T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323785T>C , CM000677.2:g.73323785T>C GRCh38
NC_000015.9:g.73616126T>C , CM000677.1:g.73616126T>C GRCh37
NC_000015.8:g.71403179T>C NCBI36
NG_009063.1:g.50480A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.2308A>G MANE Select ENSP00000261917.3:p.Thr770Ala
ENST00000261917.3:c.2308A>G ENSP00000261917.3:p.Thr770Ala
NM_005477.2:c.2308A>G NP_005468.1:p.Thr770Ala
XM_011521148.1:c.1090A>G XP_011519450.1:p.Thr364Ala
XM_011521148.2:c.1090A>G XP_011519450.1:p.Thr364Ala
NM_005477.3:c.2308A>G MANE Select NP_005468.1:p.Thr770Ala
Search 100 bp 5'
Search 100 bp 3'