Canonical Allele Identifier: CA393093606
Gene: HCN4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.73621978A>C (hg19) chr15:g.73329637A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73329637A>C , CM000677.2:g.73329637A>C GRCh38
NC_000015.9:g.73621978A>C , CM000677.1:g.73621978A>C GRCh37
NC_000015.8:g.71409031A>C NCBI36
NG_009063.1:g.44628T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.1526T>G MANE Select ENSP00000261917.3:p.Phe509Cys
ENST00000261917.3:c.1526T>G ENSP00000261917.3:p.Phe509Cys
NM_005477.2:c.1526T>G NP_005468.1:p.Phe509Cys
XM_011521148.1:c.308T>G XP_011519450.1:p.Phe103Cys
XM_011521148.2:c.308T>G XP_011519450.1:p.Phe103Cys
NM_005477.3:c.1526T>G MANE Select NP_005468.1:p.Phe509Cys
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