Canonical Allele Identifier: CA393097805
Gene: HCN4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.73660104G>T (hg19) chr15:g.73367763G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367763G>T , CM000677.2:g.73367763G>T GRCh38
NC_000015.9:g.73660104G>T , CM000677.1:g.73660104G>T GRCh37
NC_000015.8:g.71447157G>T NCBI36
NG_009063.1:g.6502C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.508C>A MANE Select ENSP00000261917.3:p.Gln170Lys
ENST00000261917.3:c.508C>A ENSP00000261917.3:p.Gln170Lys
NM_005477.2:c.508C>A NP_005468.1:p.Gln170Lys
NM_005477.3:c.508C>A MANE Select NP_005468.1:p.Gln170Lys
Search 100 bp 5'
Search 100 bp 3'