Canonical Allele Identifier: CA393089148
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs2151214815
MyVariant Identifiers: chr15:g.73616126T>G (hg19) chr15:g.73323785T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323785T>G , CM000677.2:g.73323785T>G GRCh38
NC_000015.9:g.73616126T>G , CM000677.1:g.73616126T>G GRCh37
NC_000015.8:g.71403179T>G NCBI36
NG_009063.1:g.50480A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.2308A>C MANE Select ENSP00000261917.3:p.Thr770Pro
ENST00000261917.3:c.2308A>C ENSP00000261917.3:p.Thr770Pro
NM_005477.2:c.2308A>C NP_005468.1:p.Thr770Pro
XM_011521148.1:c.1090A>C XP_011519450.1:p.Thr364Pro
XM_011521148.2:c.1090A>C XP_011519450.1:p.Thr364Pro
NM_005477.3:c.2308A>C MANE Select NP_005468.1:p.Thr770Pro
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