Canonical Allele Identifier: CA389276802
Gene: TGM1 HGNC NCBI

Linked Data

dbSNP Id: rs2040810092
gnomAD v3: 14-24261701-G-A
gnomAD v4: 14-24261701-G-A
MyVariant Identifiers: chr14:g.24730907G>A (hg19) chr14:g.24261701G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24261701G>A , CM000676.2:g.24261701G>A GRCh38
NC_000014.8:g.24730907G>A , CM000676.1:g.24730907G>A GRCh37
NC_000014.7:g.23800747G>A NCBI36
NG_007150.1:g.6466C>T
NG_007150.2:g.6466C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000206765.11:c.502C>T MANE Select ENSP00000206765.6:p.Leu168Phe
ENST00000206765.10:c.502C>T ENSP00000206765.6:p.Leu168Phe
ENST00000544573.5:c.-29+426C>T ENSP00000439446.1:n.-29+426C>T
NM_000359.2:c.502C>T NP_000350.1:p.Leu168Phe
NM_000359.3:c.502C>T MANE Select NP_000350.1:p.Leu168Phe
Search 100 bp 5'
Search 100 bp 3'