Canonical Allele Identifier: CA491477948
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs1271215764
gnomAD v3: 15-73322907-T-G
gnomAD v4: 15-73322907-T-G
MyVariant Identifiers: chr15:g.73615248T>G (hg19) chr15:g.73322907T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322907T>G , CM000677.2:g.73322907T>G GRCh38
NC_000015.9:g.73615248T>G , CM000677.1:g.73615248T>G GRCh37
NC_000015.8:g.71402301T>G NCBI36
NG_009063.1:g.51358A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3186A>C MANE Select ENSP00000261917.3:p.Pro1062=
ENST00000261917.3:c.3186A>C ENSP00000261917.3:p.Pro1062=
NM_005477.2:c.3186A>C NP_005468.1:p.Pro1062=
XM_011521148.1:c.1968A>C XP_011519450.1:p.Pro656=
XM_011521148.2:c.1968A>C XP_011519450.1:p.Pro656=
NM_005477.3:c.3186A>C MANE Select NP_005468.1:p.Pro1062=
Search 100 bp 5'
Search 100 bp 3'