Canonical Allele Identifier: CA393085384
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs2042867916

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322683G>C , CM000677.2:g.73322683G>C GRCh38
NC_000015.9:g.73615024G>C , CM000677.1:g.73615024G>C GRCh37
NC_000015.8:g.71402077G>C NCBI36
NG_009063.1:g.51582C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.3410C>G MANE Select ENSP00000261917.3:p.Pro1137Arg
ENST00000261917.3:c.3410C>G ENSP00000261917.3:p.Pro1137Arg
NM_005477.2:c.3410C>G NP_005468.1:p.Pro1137Arg
XM_011521148.1:c.2192C>G XP_011519450.1:p.Pro731Arg
XM_011521148.2:c.2192C>G XP_011519450.1:p.Pro731Arg
NM_005477.3:c.3410C>G MANE Select NP_005468.1:p.Pro1137Arg