Canonical Allele Identifier: CA393098543
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs1459039632
gnomAD v2: 15-73660346-G-A
gnomAD v3: 15-73368005-G-A
gnomAD v4: 15-73368005-G-A
MyVariant Identifiers: chr15:g.73660346G>A (hg19) chr15:g.73368005G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73368005G>A , CM000677.2:g.73368005G>A GRCh38
NC_000015.9:g.73660346G>A , CM000677.1:g.73660346G>A GRCh37
NC_000015.8:g.71447399G>A NCBI36
NG_009063.1:g.6260C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.266C>T MANE Select ENSP00000261917.3:p.Thr89Met
ENST00000261917.3:c.266C>T ENSP00000261917.3:p.Thr89Met
NM_005477.2:c.266C>T NP_005468.1:p.Thr89Met
NM_005477.3:c.266C>T MANE Select NP_005468.1:p.Thr89Met
Search 100 bp 5'
Search 100 bp 3'