Canonical Allele Identifier: CA393098233
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 937688
ClinVar RCV Id: RCV001206759
dbSNP Id: rs2043136534
gnomAD v4: 15-73367900-T-C
MyVariant Identifiers: chr15:g.73660241T>C (hg19) chr15:g.73367900T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367900T>C , CM000677.2:g.73367900T>C GRCh38
NC_000015.9:g.73660241T>C , CM000677.1:g.73660241T>C GRCh37
NC_000015.8:g.71447294T>C NCBI36
NG_009063.1:g.6365A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.371A>G MANE Select ENSP00000261917.3:p.Asp124Gly
ENST00000261917.3:c.371A>G ENSP00000261917.3:p.Asp124Gly
NM_005477.2:c.371A>G NP_005468.1:p.Asp124Gly
NM_005477.3:c.371A>G MANE Select NP_005468.1:p.Asp124Gly
Search 100 bp 5'
Search 100 bp 3'