Canonical Allele Identifier: CA715542277
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs559081867
MyVariant Identifiers: chr15:g.73614742A>C (hg19) chr15:g.73322401A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322401A>C , CM000677.2:g.73322401A>C GRCh38
NC_000015.9:g.73614742A>C , CM000677.1:g.73614742A>C GRCh37
NC_000015.8:g.71401795A>C NCBI36
NG_009063.1:g.51864T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.*80T>G MANE Select ENSP00000261917.3:n.*80T>G
ENST00000261917.3:c.*80T>G ENSP00000261917.3:n.*80T>G
NM_005477.2:c.*80T>G NP_005468.1:n.*80T>G
XM_011521148.1:c.*80T>G XP_011519450.1:n.*80T>G
XM_011521148.2:c.*80T>G XP_011519450.1:n.*80T>G
NM_005477.3:c.*80T>G MANE Select NP_005468.1:n.*80T>G
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