Canonical Allele Identifier: CA603071655
Gene: NTF3 HGNC NCBI

Linked Data

dbSNP Id: rs1037070905
gnomAD v2: 12-5597312-C-T
gnomAD v3: 12-5488146-C-T
gnomAD v4: 12-5488146-C-T
MyVariant Identifiers: chr12:g.5597312C>T (hg19) chr12:g.5488146C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.5488146C>T , CM000674.2:g.5488146C>T GRCh38
NC_000012.11:g.5597312C>T , CM000674.1:g.5597312C>T GRCh37
NC_000012.10:g.5467573C>T NCBI36
NG_050629.1:g.61033C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000423158.4:c.19-6048C>T MANE Select ENSP00000397297.2:n.19-6048C>T
ENST00000423158.3:c.19-6048C>T ENSP00000397297.2:n.19-6048C>T
ENST00000535299.5:n.232-18419C>T
ENST00000543548.1:n.209-6048C>T
NM_001102654.1:c.19-6048C>T NP_001096124.1:n.19-6048C>T
XM_011520963.1:c.-21-6048C>T XP_011519265.1:n.-21-6048C>T
XM_011520963.2:c.-21-6048C>T XP_011519265.1:n.-21-6048C>T
NM_001102654.2:c.19-6048C>T MANE Select NP_001096124.1:n.19-6048C>T
Search 100 bp 5'
Search 100 bp 3'