Canonical Allele Identifier: CA2629370933
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs2151214986
gnomAD v4: 15-73324035-G-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73324035G>T , CM000677.2:g.73324035G>T GRCh38
NC_000015.9:g.73616376G>T , CM000677.1:g.73616376G>T GRCh37
NC_000015.8:g.71403429G>T NCBI36
NG_009063.1:g.50230C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.2143+54C>A MANE Select ENSP00000261917.3:n.2143+54C>A
ENST00000261917.3:c.2143+54C>A ENSP00000261917.3:n.2143+54C>A
NM_005477.2:c.2143+54C>A NP_005468.1:n.2143+54C>A
XM_011521148.1:c.925+54C>A XP_011519450.1:n.925+54C>A
XM_011521148.2:c.925+54C>A XP_011519450.1:n.925+54C>A
NM_005477.3:c.2143+54C>A MANE Select NP_005468.1:n.2143+54C>A
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