Canonical Allele Identifier: CA491478125
Gene: HCN4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.73615353G>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323012G>C , CM000677.2:g.73323012G>C GRCh38
NC_000015.9:g.73615353G>C , CM000677.1:g.73615353G>C GRCh37
NC_000015.8:g.71402406G>C NCBI36
NG_009063.1:g.51253C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3081C>G MANE Select ENSP00000261917.3:p.Pro1027=
ENST00000261917.3:c.3081C>G ENSP00000261917.3:p.Pro1027=
NM_005477.2:c.3081C>G NP_005468.1:p.Pro1027=
XM_011521148.1:c.1863C>G XP_011519450.1:p.Pro621=
XM_011521148.2:c.1863C>G XP_011519450.1:p.Pro621=
NM_005477.3:c.3081C>G MANE Select NP_005468.1:p.Pro1027=
Search 100 bp 5'
Search 100 bp 3'