Canonical Allele Identifier: CA2013631919
Gene: NTF3 HGNC NCBI

Linked Data

dbSNP Id: rs1565397183
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.5488155G>A , CM000674.2:g.5488155G>A GRCh38
NC_000012.11:g.5597321G>A , CM000674.1:g.5597321G>A GRCh37
NC_000012.10:g.5467582G>A NCBI36
NG_050629.1:g.61042G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000423158.4:c.19-6039G>A MANE Select ENSP00000397297.2:n.19-6039G>A
ENST00000423158.3:c.19-6039G>A ENSP00000397297.2:n.19-6039G>A
ENST00000535299.5:n.232-18410G>A
ENST00000543548.1:n.209-6039G>A
NM_001102654.1:c.19-6039G>A NP_001096124.1:n.19-6039G>A
XM_011520963.1:c.-21-6039G>A XP_011519265.1:n.-21-6039G>A
XM_011520963.2:c.-21-6039G>A XP_011519265.1:n.-21-6039G>A
NM_001102654.2:c.19-6039G>A MANE Select NP_001096124.1:n.19-6039G>A
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