Canonical Allele Identifier: CA393089157
Gene: HCN4 HGNC NCBI

Linked Data

gnomAD v4: 15-73323791-T-C
MyVariant Identifiers: chr15:g.73616132T>C (hg19) chr15:g.73323791T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323791T>C , CM000677.2:g.73323791T>C GRCh38
NC_000015.9:g.73616132T>C , CM000677.1:g.73616132T>C GRCh37
NC_000015.8:g.71403185T>C NCBI36
NG_009063.1:g.50474A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.2302A>G MANE Select ENSP00000261917.3:p.Thr768Ala
ENST00000261917.3:c.2302A>G ENSP00000261917.3:p.Thr768Ala
NM_005477.2:c.2302A>G NP_005468.1:p.Thr768Ala
XM_011521148.1:c.1084A>G XP_011519450.1:p.Thr362Ala
XM_011521148.2:c.1084A>G XP_011519450.1:p.Thr362Ala
NM_005477.3:c.2302A>G MANE Select NP_005468.1:p.Thr768Ala
Search 100 bp 5'
Search 100 bp 3'