Canonical Allele Identifier: CA231871881
Gene: NTF3 HGNC NCBI

Linked Data

dbSNP Id: rs976380167
MyVariant Identifiers: chr12:g.5597299T>C (hg19) chr12:g.5488133T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.5488133T>C , CM000674.2:g.5488133T>C GRCh38
NC_000012.11:g.5597299T>C , CM000674.1:g.5597299T>C GRCh37
NC_000012.10:g.5467560T>C NCBI36
NG_050629.1:g.61020T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000423158.4:c.19-6061T>C MANE Select ENSP00000397297.2:n.19-6061T>C
ENST00000423158.3:c.19-6061T>C ENSP00000397297.2:n.19-6061T>C
ENST00000535299.5:n.232-18432T>C
ENST00000543548.1:n.209-6061T>C
NM_001102654.1:c.19-6061T>C NP_001096124.1:n.19-6061T>C
XM_011520963.1:c.-21-6061T>C XP_011519265.1:n.-21-6061T>C
XM_011520963.2:c.-21-6061T>C XP_011519265.1:n.-21-6061T>C
NM_001102654.2:c.19-6061T>C MANE Select NP_001096124.1:n.19-6061T>C
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