Canonical Allele Identifier: CA7649003
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs772267234
ExAC: 15:73615893 G / A
gnomAD v2: 15-73615893-G-A
gnomAD v4: 15-73323552-G-A
MyVariant Identifiers: chr15:g.73615893G>A (hg19) chr15:g.73323552G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323552G>A , CM000677.2:g.73323552G>A GRCh38
NC_000015.9:g.73615893G>A , CM000677.1:g.73615893G>A GRCh37
NC_000015.8:g.71402946G>A NCBI36
NG_009063.1:g.50713C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.2541C>T MANE Select ENSP00000261917.3:p.Ser847=
ENST00000261917.3:c.2541C>T ENSP00000261917.3:p.Ser847=
NM_005477.2:c.2541C>T NP_005468.1:p.Ser847=
XM_011521148.1:c.1323C>T XP_011519450.1:p.Ser441=
XM_011521148.2:c.1323C>T XP_011519450.1:p.Ser441=
NM_005477.3:c.2541C>T MANE Select NP_005468.1:p.Ser847=
Search 100 bp 5'
Search 100 bp 3'