Canonical Allele Identifier: CA7649492
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs770361300
ExAC: 15:73660364 C / A
gnomAD v2: 15-73660364-C-A
gnomAD v4: 15-73368023-C-A
MyVariant Identifiers: chr15:g.73660364C>A (hg19) chr15:g.73368023C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73368023C>A , CM000677.2:g.73368023C>A GRCh38
NC_000015.9:g.73660364C>A , CM000677.1:g.73660364C>A GRCh37
NC_000015.8:g.71447417C>A NCBI36
NG_009063.1:g.6242G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.248G>T MANE Select ENSP00000261917.3:p.Gly83Val
ENST00000261917.3:c.248G>T ENSP00000261917.3:p.Gly83Val
NM_005477.2:c.248G>T NP_005468.1:p.Gly83Val
NM_005477.3:c.248G>T MANE Select NP_005468.1:p.Gly83Val
Search 100 bp 5'
Search 100 bp 3'