Canonical Allele Identifier: CA7649445
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1753366
ClinVar RCV Id: RCV002361609
dbSNP Id: rs762586116
ExAC: 15:73659972 T / A
gnomAD v2: 15-73659972-T-A
gnomAD v4: 15-73367631-T-A
MyVariant Identifiers: chr15:g.73659972T>A (hg19) chr15:g.73367631T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367631T>A , CM000677.2:g.73367631T>A GRCh38
NC_000015.9:g.73659972T>A , CM000677.1:g.73659972T>A GRCh37
NC_000015.8:g.71447025T>A NCBI36
NG_009063.1:g.6634A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.640A>T MANE Select ENSP00000261917.3:p.Met214Leu
ENST00000261917.3:c.640A>T ENSP00000261917.3:p.Met214Leu
NM_005477.2:c.640A>T NP_005468.1:p.Met214Leu
NM_005477.3:c.640A>T MANE Select NP_005468.1:p.Met214Leu
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Search 100 bp 3'