Canonical Allele Identifier: CA491478477
Gene: HCN4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.73615734G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323393G>C , CM000677.2:g.73323393G>C GRCh38
NC_000015.9:g.73615734G>C , CM000677.1:g.73615734G>C GRCh37
NC_000015.8:g.71402787G>C NCBI36
NG_009063.1:g.50872C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.2700C>G MANE Select ENSP00000261917.3:p.Ala900=
ENST00000261917.3:c.2700C>G ENSP00000261917.3:p.Ala900=
NM_005477.2:c.2700C>G NP_005468.1:p.Ala900=
XM_011521148.1:c.1482C>G XP_011519450.1:p.Ala494=
XM_011521148.2:c.1482C>G XP_011519450.1:p.Ala494=
NM_005477.3:c.2700C>G MANE Select NP_005468.1:p.Ala900=
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