Canonical Allele Identifier: CA7648910
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1063989
ClinVar RCV Id: RCV001373892 RCV004037589
dbSNP Id: rs761666368
ExAC: 15:73615442 G / C
gnomAD v2: 15-73615442-G-C
gnomAD v4: 15-73323101-G-C
MyVariant Identifiers: chr15:g.73615442G>C (hg19) chr15:g.73323101G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323101G>C , CM000677.2:g.73323101G>C GRCh38
NC_000015.9:g.73615442G>C , CM000677.1:g.73615442G>C GRCh37
NC_000015.8:g.71402495G>C NCBI36
NG_009063.1:g.51164C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.2992C>G MANE Select ENSP00000261917.3:p.Pro998Ala
ENST00000261917.3:c.2992C>G ENSP00000261917.3:p.Pro998Ala
NM_005477.2:c.2992C>G NP_005468.1:p.Pro998Ala
XM_011521148.1:c.1774C>G XP_011519450.1:p.Pro592Ala
XM_011521148.2:c.1774C>G XP_011519450.1:p.Pro592Ala
NM_005477.3:c.2992C>G MANE Select NP_005468.1:p.Pro998Ala
Search 100 bp 5'
Search 100 bp 3'