Canonical Allele Identifier: CA393098732
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs1595837618
gnomAD v4: 15-73368071-G-T
MyVariant Identifiers: chr15:g.73660412G>T (hg19) chr15:g.73368071G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73368071G>T , CM000677.2:g.73368071G>T GRCh38
NC_000015.9:g.73660412G>T , CM000677.1:g.73660412G>T GRCh37
NC_000015.8:g.71447465G>T NCBI36
NG_009063.1:g.6194C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.200C>A MANE Select ENSP00000261917.3:p.Ser67Tyr
ENST00000261917.3:c.200C>A ENSP00000261917.3:p.Ser67Tyr
NM_005477.2:c.200C>A NP_005468.1:p.Ser67Tyr
NM_005477.3:c.200C>A MANE Select NP_005468.1:p.Ser67Tyr
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