Canonical Allele Identifier: CA393095027
Community Standard Title: NM_005477.3(HCN4):c.1020C>G (p.Ser340Arg)
Gene: HCN4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73343574G>C , CM000677.2:g.73343574G>C GRCh38
NC_000015.9:g.73635915G>C , CM000677.1:g.73635915G>C GRCh37
NC_000015.8:g.71422968G>C NCBI36
NG_009063.1:g.30691C>G

Transcript Alleles

HGVS Amino-acid Change
NM_005477.3:c.1020C>G MANE Select NP_005468.1:p.Ser340Arg
ENST00000261917.4:c.1020C>G MANE Select ENSP00000261917.3:p.Ser340Arg
NM_005477.2:c.1020C>G NP_005468.1:p.Ser340Arg
ENST00000261917.3:c.1020C>G ENSP00000261917.3:p.Ser340Arg
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