Canonical Allele Identifier: CA393085266
Gene: HCN4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.73614983T>C (hg19) chr15:g.73322642T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322642T>C , CM000677.2:g.73322642T>C GRCh38
NC_000015.9:g.73614983T>C , CM000677.1:g.73614983T>C GRCh37
NC_000015.8:g.71402036T>C NCBI36
NG_009063.1:g.51623A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3451A>G MANE Select ENSP00000261917.3:p.Thr1151Ala
ENST00000261917.3:c.3451A>G ENSP00000261917.3:p.Thr1151Ala
NM_005477.2:c.3451A>G NP_005468.1:p.Thr1151Ala
XM_011521148.1:c.2233A>G XP_011519450.1:p.Thr745Ala
XM_011521148.2:c.2233A>G XP_011519450.1:p.Thr745Ala
NM_005477.3:c.3451A>G MANE Select NP_005468.1:p.Thr1151Ala
Search 100 bp 5'
Search 100 bp 3'