Canonical Allele Identifier: CA393097811
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs1303993591
gnomAD v2: 15-73660106-T-G
gnomAD v4: 15-73367765-T-G
MyVariant Identifiers: chr15:g.73660106T>G (hg19) chr15:g.73367765T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367765T>G , CM000677.2:g.73367765T>G GRCh38
NC_000015.9:g.73660106T>G , CM000677.1:g.73660106T>G GRCh37
NC_000015.8:g.71447159T>G NCBI36
NG_009063.1:g.6500A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.506A>C MANE Select ENSP00000261917.3:p.Gln169Pro
ENST00000261917.3:c.506A>C ENSP00000261917.3:p.Gln169Pro
NM_005477.2:c.506A>C NP_005468.1:p.Gln169Pro
NM_005477.3:c.506A>C MANE Select NP_005468.1:p.Gln169Pro
Search 100 bp 5'
Search 100 bp 3'