Canonical Allele Identifier: CA2187188908
Gene: HCN4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73324031C= , CM000677.2:g.73324031C= GRCh38
NC_000015.9:g.73616372C= , CM000677.1:g.73616372C= GRCh37
NC_000015.8:g.71403425C= NCBI36
NG_009063.1:g.50234G=

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.2143+58G= MANE Select ENSP00000261917.3:n.2143+58G=
ENST00000261917.3:c.2143+58G= ENSP00000261917.3:n.2143+58G=
NM_005477.2:c.2143+58G= NP_005468.1:n.2143+58G=
XM_011521148.1:c.925+58G= XP_011519450.1:n.925+58G=
XM_011521148.2:c.925+58G= XP_011519450.1:n.925+58G=
NM_005477.3:c.2143+58G= MANE Select NP_005468.1:n.2143+58G=
Search 100 bp 5'
Search 100 bp 3'