Canonical Allele Identifier: CA491478116
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1116893
ClinVar RCV Id: RCV001445453
dbSNP Id: rs1280129625
gnomAD v2: 15-73615347-G-A
gnomAD v4: 15-73323006-G-A
MyVariant Identifiers: chr15:g.73615347G>A (hg19) chr15:g.73323006G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323006G>A , CM000677.2:g.73323006G>A GRCh38
NC_000015.9:g.73615347G>A , CM000677.1:g.73615347G>A GRCh37
NC_000015.8:g.71402400G>A NCBI36
NG_009063.1:g.51259C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.3087C>T MANE Select ENSP00000261917.3:p.Gly1029=
ENST00000261917.3:c.3087C>T ENSP00000261917.3:p.Gly1029=
NM_005477.2:c.3087C>T NP_005468.1:p.Gly1029=
XM_011521148.1:c.1869C>T XP_011519450.1:p.Gly623=
XM_011521148.2:c.1869C>T XP_011519450.1:p.Gly623=
NM_005477.3:c.3087C>T MANE Select NP_005468.1:p.Gly1029=
Search 100 bp 5'
Search 100 bp 3'