Canonical Allele Identifier: CA7649054
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs757482655
ExAC: 15:73616130 G / T
gnomAD v2: 15-73616130-G-T
gnomAD v4: 15-73323789-G-T
MyVariant Identifiers: chr15:g.73616130G>T (hg19) chr15:g.73323789G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323789G>T , CM000677.2:g.73323789G>T GRCh38
NC_000015.9:g.73616130G>T , CM000677.1:g.73616130G>T GRCh37
NC_000015.8:g.71403183G>T NCBI36
NG_009063.1:g.50476C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.2304C>A MANE Select ENSP00000261917.3:p.Thr768=
ENST00000261917.3:c.2304C>A ENSP00000261917.3:p.Thr768=
NM_005477.2:c.2304C>A NP_005468.1:p.Thr768=
XM_011521148.1:c.1086C>A XP_011519450.1:p.Thr362=
XM_011521148.2:c.1086C>A XP_011519450.1:p.Thr362=
NM_005477.3:c.2304C>A MANE Select NP_005468.1:p.Thr768=
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