Canonical Allele Identifier: CA7648907
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs749040050
ExAC: 15:73615437 C / G
gnomAD v2: 15-73615437-C-G
gnomAD v4: 15-73323096-C-G
MyVariant Identifiers: chr15:g.73615437C>G (hg19) chr15:g.73323096C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323096C>G , CM000677.2:g.73323096C>G GRCh38
NC_000015.9:g.73615437C>G , CM000677.1:g.73615437C>G GRCh37
NC_000015.8:g.71402490C>G NCBI36
NG_009063.1:g.51169G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.2997G>C MANE Select ENSP00000261917.3:p.Arg999=
ENST00000261917.3:c.2997G>C ENSP00000261917.3:p.Arg999=
NM_005477.2:c.2997G>C NP_005468.1:p.Arg999=
XM_011521148.1:c.1779G>C XP_011519450.1:p.Arg593=
XM_011521148.2:c.1779G>C XP_011519450.1:p.Arg593=
NM_005477.3:c.2997G>C MANE Select NP_005468.1:p.Arg999=
Search 100 bp 5'
Search 100 bp 3'