Canonical Allele Identifier: CA393088710
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1026190
ClinVar RCV Id: RCV001326611
dbSNP Id: rs2042878358
MyVariant Identifiers: chr15:g.73615900C>G (hg19) chr15:g.73323559C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323559C>G , CM000677.2:g.73323559C>G GRCh38
NC_000015.9:g.73615900C>G , CM000677.1:g.73615900C>G GRCh37
NC_000015.8:g.71402953C>G NCBI36
NG_009063.1:g.50706G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.2534G>C MANE Select ENSP00000261917.3:p.Ser845Thr
ENST00000261917.3:c.2534G>C ENSP00000261917.3:p.Ser845Thr
NM_005477.2:c.2534G>C NP_005468.1:p.Ser845Thr
XM_011521148.1:c.1316G>C XP_011519450.1:p.Ser439Thr
XM_011521148.2:c.1316G>C XP_011519450.1:p.Ser439Thr
NM_005477.3:c.2534G>C MANE Select NP_005468.1:p.Ser845Thr
Search 100 bp 5'
Search 100 bp 3'