Canonical Allele Identifier: CA393093625
Gene: HCN4 HGNC NCBI

Linked Data

gnomAD v4: 15-73329640-A-G
MyVariant Identifiers: chr15:g.73621981A>G (hg19) chr15:g.73329640A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73329640A>G , CM000677.2:g.73329640A>G GRCh38
NC_000015.9:g.73621981A>G , CM000677.1:g.73621981A>G GRCh37
NC_000015.8:g.71409034A>G NCBI36
NG_009063.1:g.44625T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.1523T>C MANE Select ENSP00000261917.3:p.Met508Thr
ENST00000261917.3:c.1523T>C ENSP00000261917.3:p.Met508Thr
NM_005477.2:c.1523T>C NP_005468.1:p.Met508Thr
XM_011521148.1:c.305T>C XP_011519450.1:p.Met102Thr
XM_011521148.2:c.305T>C XP_011519450.1:p.Met102Thr
NM_005477.3:c.1523T>C MANE Select NP_005468.1:p.Met508Thr
Search 100 bp 5'
Search 100 bp 3'