Canonical Allele Identifier: CA393093754
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs1330225452
gnomAD v3: 15-73329671-T-G
gnomAD v4: 15-73329671-T-G
MyVariant Identifiers: chr15:g.73622012T>G (hg19) chr15:g.73329671T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73329671T>G , CM000677.2:g.73329671T>G GRCh38
NC_000015.9:g.73622012T>G , CM000677.1:g.73622012T>G GRCh37
NC_000015.8:g.71409065T>G NCBI36
NG_009063.1:g.44594A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.1492A>C MANE Select ENSP00000261917.3:p.Ser498Arg
ENST00000261917.3:c.1492A>C ENSP00000261917.3:p.Ser498Arg
NM_005477.2:c.1492A>C NP_005468.1:p.Ser498Arg
XM_011521148.1:c.274A>C XP_011519450.1:p.Ser92Arg
XM_011521148.2:c.274A>C XP_011519450.1:p.Ser92Arg
NM_005477.3:c.1492A>C MANE Select NP_005468.1:p.Ser498Arg
Search 100 bp 5'
Search 100 bp 3'