Canonical Allele Identifier: CA393097621
Gene: HCN4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.73660047T>A (hg19) chr15:g.73367706T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367706T>A , CM000677.2:g.73367706T>A GRCh38
NC_000015.9:g.73660047T>A , CM000677.1:g.73660047T>A GRCh37
NC_000015.8:g.71447100T>A NCBI36
NG_009063.1:g.6559A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.565A>T MANE Select ENSP00000261917.3:p.Lys189Ter
ENST00000261917.3:c.565A>T ENSP00000261917.3:p.Lys189Ter
NM_005477.2:c.565A>T NP_005468.1:p.Lys189Ter
NM_005477.3:c.565A>T MANE Select NP_005468.1:p.Lys189Ter
Search 100 bp 5'
Search 100 bp 3'