Canonical Allele Identifier: CA393097382
Gene: HCN4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.73659970C>G (hg19) chr15:g.73367629C>G (hg38)
JSON-LD

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.642G>C MANE Select ENSP00000261917.3:p.Met214Ile
ENST00000261917.3:c.642G>C ENSP00000261917.3:p.Met214Ile
NM_005477.2:c.642G>C NP_005468.1:p.Met214Ile
NM_005477.3:c.642G>C MANE Select NP_005468.1:p.Met214Ile
Search 100 bp 5'
Search 100 bp 3'