Canonical Allele Identifier: CA393098129
Gene: HCN4 HGNC NCBI

Linked Data

gnomAD v4: 15-73367868-C-G
MyVariant Identifiers: chr15:g.73660209C>G (hg19) chr15:g.73367868C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367868C>G , CM000677.2:g.73367868C>G GRCh38
NC_000015.9:g.73660209C>G , CM000677.1:g.73660209C>G GRCh37
NC_000015.8:g.71447262C>G NCBI36
NG_009063.1:g.6397G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.403G>C MANE Select ENSP00000261917.3:p.Gly135Arg
ENST00000261917.3:c.403G>C ENSP00000261917.3:p.Gly135Arg
NM_005477.2:c.403G>C NP_005468.1:p.Gly135Arg
NM_005477.3:c.403G>C MANE Select NP_005468.1:p.Gly135Arg
Search 100 bp 5'
Search 100 bp 3'