Canonical Allele Identifier: CA2187194491
Gene: HCN4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367674C= , CM000677.2:g.73367674C= GRCh38
NC_000015.9:g.73660015C= , CM000677.1:g.73660015C= GRCh37
NC_000015.8:g.71447068C= NCBI36
NG_009063.1:g.6591G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.597G= MANE Select ENSP00000261917.3:p.Gln199=
ENST00000261917.3:c.597G= ENSP00000261917.3:p.Gln199=
NM_005477.2:c.597G= NP_005468.1:p.Gln199=
NM_005477.3:c.597G= MANE Select NP_005468.1:p.Gln199=
Search 100 bp 5'
Search 100 bp 3'