Canonical Allele Identifier: CA612959133
Gene: TGM1 HGNC NCBI

Linked Data

dbSNP Id: rs1376223641
gnomAD v2: 14-24725176-C-A
gnomAD v4: 14-24255970-C-A
MyVariant Identifiers: chr14:g.24725176C>A (hg19) chr14:g.24255970C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24255970C>A , CM000676.2:g.24255970C>A GRCh38
NC_000014.8:g.24725176C>A , CM000676.1:g.24725176C>A GRCh37
NC_000014.7:g.23795016C>A NCBI36
NG_007150.1:g.12197G>T
NG_007150.2:g.12197G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000206765.11:c.1491+19G>T MANE Select ENSP00000206765.6:n.1491+19G>T
ENST00000206765.10:c.1491+19G>T ENSP00000206765.6:n.1491+19G>T
ENST00000544573.5:c.165+19G>T ENSP00000439446.1:n.165+19G>T
ENST00000559136.1:c.564+19G>T ENSP00000453337.1:n.564+19G>T
NM_000359.2:c.1491+19G>T NP_000350.1:n.1491+19G>T
NM_000359.3:c.1491+19G>T MANE Select NP_000350.1:n.1491+19G>T
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