Canonical Allele Identifier: CA7649476
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2565011
ClinVar RCV Id: RCV003297366 RCV003505326
dbSNP Id: rs761237260
ExAC: 15:73660197 G / C
gnomAD v2: 15-73660197-G-C
gnomAD v4: 15-73367856-G-C
MyVariant Identifiers: chr15:g.73660197G>C (hg19) chr15:g.73367856G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367856G>C , CM000677.2:g.73367856G>C GRCh38
NC_000015.9:g.73660197G>C , CM000677.1:g.73660197G>C GRCh37
NC_000015.8:g.71447250G>C NCBI36
NG_009063.1:g.6409C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.415C>G MANE Select ENSP00000261917.3:p.Pro139Ala
ENST00000261917.3:c.415C>G ENSP00000261917.3:p.Pro139Ala
NM_005477.2:c.415C>G NP_005468.1:p.Pro139Ala
NM_005477.3:c.415C>G MANE Select NP_005468.1:p.Pro139Ala
Search 100 bp 5'
Search 100 bp 3'