Canonical Allele Identifier: CA715546914
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs1435390380
MyVariant Identifiers: chr15:g.73616365A>G (hg19) chr15:g.73324024A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73324024A>G , CM000677.2:g.73324024A>G GRCh38
NC_000015.9:g.73616365A>G , CM000677.1:g.73616365A>G GRCh37
NC_000015.8:g.71403418A>G NCBI36
NG_009063.1:g.50241T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.2143+65T>C MANE Select ENSP00000261917.3:n.2143+65T>C
ENST00000261917.3:c.2143+65T>C ENSP00000261917.3:n.2143+65T>C
NM_005477.2:c.2143+65T>C NP_005468.1:n.2143+65T>C
XM_011521148.1:c.925+65T>C XP_011519450.1:n.925+65T>C
XM_011521148.2:c.925+65T>C XP_011519450.1:n.925+65T>C
NM_005477.3:c.2143+65T>C MANE Select NP_005468.1:n.2143+65T>C
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