Canonical Allele Identifier: CA393089158
Gene: HCN4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.73616132T>G (hg19) chr15:g.73323791T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323791T>G , CM000677.2:g.73323791T>G GRCh38
NC_000015.9:g.73616132T>G , CM000677.1:g.73616132T>G GRCh37
NC_000015.8:g.71403185T>G NCBI36
NG_009063.1:g.50474A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.2302A>C MANE Select ENSP00000261917.3:p.Thr768Pro
ENST00000261917.3:c.2302A>C ENSP00000261917.3:p.Thr768Pro
NM_005477.2:c.2302A>C NP_005468.1:p.Thr768Pro
XM_011521148.1:c.1084A>C XP_011519450.1:p.Thr362Pro
XM_011521148.2:c.1084A>C XP_011519450.1:p.Thr362Pro
NM_005477.3:c.2302A>C MANE Select NP_005468.1:p.Thr768Pro
Search 100 bp 5'
Search 100 bp 3'