Canonical Allele Identifier: CA2595918237
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs2151228810
gnomAD v3: 15-73368273-C-T
gnomAD v4: 15-73368273-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73368273C>T , CM000677.2:g.73368273C>T GRCh38
NC_000015.9:g.73660614C>T , CM000677.1:g.73660614C>T GRCh37
NC_000015.8:g.71447667C>T NCBI36
NG_009063.1:g.5992G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.-3G>A MANE Select ENSP00000261917.3:n.-3G>A
ENST00000261917.3:c.-3G>A ENSP00000261917.3:n.-3G>A
NM_005477.2:c.-3G>A NP_005468.1:n.-3G>A
NM_005477.3:c.-3G>A MANE Select NP_005468.1:n.-3G>A
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