Canonical Allele Identifier: CA2187167364
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs1595822862
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73329566G>A , CM000677.2:g.73329566G>A GRCh38
NC_000015.9:g.73621907G>A , CM000677.1:g.73621907G>A GRCh37
NC_000015.8:g.71408960G>A NCBI36
NG_009063.1:g.44699C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.1590+7C>T MANE Select ENSP00000261917.3:n.1590+7C>T
ENST00000261917.3:c.1590+7C>T ENSP00000261917.3:n.1590+7C>T
NM_005477.2:c.1590+7C>T NP_005468.1:n.1590+7C>T
XM_011521148.1:c.372+7C>T XP_011519450.1:n.372+7C>T
XM_011521148.2:c.372+7C>T XP_011519450.1:n.372+7C>T
NM_005477.3:c.1590+7C>T MANE Select NP_005468.1:n.1590+7C>T
Search 100 bp 5'
Search 100 bp 3'