Canonical Allele Identifier: CA971407255
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs2042936233
gnomAD v3: 15-73332043-C-T
gnomAD v4: 15-73332043-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73332043C>T , CM000677.2:g.73332043C>T GRCh38
NC_000015.9:g.73624384C>T , CM000677.1:g.73624384C>T GRCh37
NC_000015.8:g.71411437C>T NCBI36
NG_009063.1:g.42222G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.1371+88G>A MANE Select ENSP00000261917.3:n.1371+88G>A
ENST00000261917.3:c.1371+88G>A ENSP00000261917.3:n.1371+88G>A
NM_005477.2:c.1371+88G>A NP_005468.1:n.1371+88G>A
XM_011521148.1:c.153+88G>A XP_011519450.1:n.153+88G>A
XM_011521148.2:c.153+88G>A XP_011519450.1:n.153+88G>A
NM_005477.3:c.1371+88G>A MANE Select NP_005468.1:n.1371+88G>A
Search 100 bp 5'
Search 100 bp 3'