Canonical Allele Identifier: CA393093718
Gene: HCN4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.73622002A>C (hg19) chr15:g.73329661A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73329661A>C , CM000677.2:g.73329661A>C GRCh38
NC_000015.9:g.73622002A>C , CM000677.1:g.73622002A>C GRCh37
NC_000015.8:g.71409055A>C NCBI36
NG_009063.1:g.44604T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.1502T>G MANE Select ENSP00000261917.3:p.Val501Gly
ENST00000261917.3:c.1502T>G ENSP00000261917.3:p.Val501Gly
NM_005477.2:c.1502T>G NP_005468.1:p.Val501Gly
XM_011521148.1:c.284T>G XP_011519450.1:p.Val95Gly
XM_011521148.2:c.284T>G XP_011519450.1:p.Val95Gly
NM_005477.3:c.1502T>G MANE Select NP_005468.1:p.Val501Gly
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Search 100 bp 3'