Canonical Allele Identifier: CA393093775
Gene: HCN4 HGNC NCBI

Linked Data

gnomAD v4: 15-73329680-T-C
MyVariant Identifiers: chr15:g.73622021T>C (hg19) chr15:g.73329680T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73329680T>C , CM000677.2:g.73329680T>C GRCh38
NC_000015.9:g.73622021T>C , CM000677.1:g.73622021T>C GRCh37
NC_000015.8:g.71409074T>C NCBI36
NG_009063.1:g.44585A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.1483A>G MANE Select ENSP00000261917.3:p.Thr495Ala
ENST00000261917.3:c.1483A>G ENSP00000261917.3:p.Thr495Ala
NM_005477.2:c.1483A>G NP_005468.1:p.Thr495Ala
XM_011521148.1:c.265A>G XP_011519450.1:p.Thr89Ala
XM_011521148.2:c.265A>G XP_011519450.1:p.Thr89Ala
NM_005477.3:c.1483A>G MANE Select NP_005468.1:p.Thr495Ala
Search 100 bp 5'
Search 100 bp 3'