Canonical Allele Identifier: CA491478339
Gene: HCN4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.73616130G>C (hg19)
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Genomic Alleles

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

Transcript Alleles

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