Canonical Allele Identifier: CA272663259
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs773914774
gnomAD v4: 15-73322684-G-T
MyVariant Identifiers: chr15:g.73615025G>T (hg19) chr15:g.73322684G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322684G>T , CM000677.2:g.73322684G>T GRCh38
NC_000015.9:g.73615025G>T , CM000677.1:g.73615025G>T GRCh37
NC_000015.8:g.71402078G>T NCBI36
NG_009063.1:g.51581C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.3409C>A MANE Select ENSP00000261917.3:p.Pro1137Thr
ENST00000261917.3:c.3409C>A ENSP00000261917.3:p.Pro1137Thr
NM_005477.2:c.3409C>A NP_005468.1:p.Pro1137Thr
XM_011521148.1:c.2191C>A XP_011519450.1:p.Pro731Thr
XM_011521148.2:c.2191C>A XP_011519450.1:p.Pro731Thr
NM_005477.3:c.3409C>A MANE Select NP_005468.1:p.Pro1137Thr
Search 100 bp 5'
Search 100 bp 3'