Canonical Allele Identifier: CA7649444
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs752207061
ExAC: 15:73659970 C / A
gnomAD v2: 15-73659970-C-A
gnomAD v4: 15-73367629-C-A
MyVariant Identifiers: chr15:g.73659970C>A (hg19) chr15:g.73367629C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367629C>A , CM000677.2:g.73367629C>A GRCh38
NC_000015.9:g.73659970C>A , CM000677.1:g.73659970C>A GRCh37
NC_000015.8:g.71447023C>A NCBI36
NG_009063.1:g.6636G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.642G>T MANE Select ENSP00000261917.3:p.Met214Ile
ENST00000261917.3:c.642G>T ENSP00000261917.3:p.Met214Ile
NM_005477.2:c.642G>T NP_005468.1:p.Met214Ile
NM_005477.3:c.642G>T MANE Select NP_005468.1:p.Met214Ile
Search 100 bp 5'
Search 100 bp 3'