Canonical Allele Identifier: CA7648793
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs542636933
ExAC: 15:73614835 G / T
gnomAD v2: 15-73614835-G-T
gnomAD v4: 15-73322494-G-T
MyVariant Identifiers: chr15:g.73614835G>T (hg19) chr15:g.73322494G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322494G>T , CM000677.2:g.73322494G>T GRCh38
NC_000015.9:g.73614835G>T , CM000677.1:g.73614835G>T GRCh37
NC_000015.8:g.71401888G>T NCBI36
NG_009063.1:g.51771C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3599C>A MANE Select ENSP00000261917.3:p.Pro1200Gln
ENST00000261917.3:c.3599C>A ENSP00000261917.3:p.Pro1200Gln
NM_005477.2:c.3599C>A NP_005468.1:p.Pro1200Gln
XM_011521148.1:c.2381C>A XP_011519450.1:p.Pro794Gln
XM_011521148.2:c.2381C>A XP_011519450.1:p.Pro794Gln
NM_005477.3:c.3599C>A MANE Select NP_005468.1:p.Pro1200Gln
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