Canonical Allele Identifier: CA272664854
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs767187346
MyVariant Identifiers: chr15:g.73616054C>T (hg19) chr15:g.73323713C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323713C>T , CM000677.2:g.73323713C>T GRCh38
NC_000015.9:g.73616054C>T , CM000677.1:g.73616054C>T GRCh37
NC_000015.8:g.71403107C>T NCBI36
NG_009063.1:g.50552G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.2380G>A MANE Select ENSP00000261917.3:p.Ala794Thr
ENST00000261917.3:c.2380G>A ENSP00000261917.3:p.Ala794Thr
NM_005477.2:c.2380G>A NP_005468.1:p.Ala794Thr
XM_011521148.1:c.1162G>A XP_011519450.1:p.Ala388Thr
XM_011521148.2:c.1162G>A XP_011519450.1:p.Ala388Thr
NM_005477.3:c.2380G>A MANE Select NP_005468.1:p.Ala794Thr
Search 100 bp 5'
Search 100 bp 3'