Canonical Allele Identifier: CA393099269
Gene: HCN4 HGNC NCBI

Linked Data

gnomAD v4: 15-73368255-G-T
MyVariant Identifiers: chr15:g.73660596G>T (hg19) chr15:g.73368255G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73368255G>T , CM000677.2:g.73368255G>T GRCh38
NC_000015.9:g.73660596G>T , CM000677.1:g.73660596G>T GRCh37
NC_000015.8:g.71447649G>T NCBI36
NG_009063.1:g.6010C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.16C>A MANE Select ENSP00000261917.3:p.Pro6Thr
ENST00000261917.3:c.16C>A ENSP00000261917.3:p.Pro6Thr
NM_005477.2:c.16C>A NP_005468.1:p.Pro6Thr
NM_005477.3:c.16C>A MANE Select NP_005468.1:p.Pro6Thr
Search 100 bp 5'
Search 100 bp 3'