Canonical Allele Identifier: CA393094335
Gene: HCN4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.73624515T>G (hg19) chr15:g.73332174T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73332174T>G , CM000677.2:g.73332174T>G GRCh38
NC_000015.9:g.73624515T>G , CM000677.1:g.73624515T>G GRCh37
NC_000015.8:g.71411568T>G NCBI36
NG_009063.1:g.42091A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.1328A>C MANE Select ENSP00000261917.3:p.Gln443Pro
ENST00000261917.3:c.1328A>C ENSP00000261917.3:p.Gln443Pro
NM_005477.2:c.1328A>C NP_005468.1:p.Gln443Pro
XM_011521148.1:c.110A>C XP_011519450.1:p.Gln37Pro
XM_011521148.2:c.110A>C XP_011519450.1:p.Gln37Pro
NM_005477.3:c.1328A>C MANE Select NP_005468.1:p.Gln443Pro
Search 100 bp 5'
Search 100 bp 3'