Canonical Allele Identifier: CA608741266

Gene: PDX1

Linked Data

• dbSNP Id: rs1280696225
• gnomAD v2: 13-28498881-C-T
• gnomAD v3: 13-27924744-C-T
• gnomAD v4: 13-27924744-C-T
• MyVariant Identifiers: chr13:g.28498881C>T (hg19) ; chr13:g.27924744C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.27924744C>T , CM000675.2:g.27924744C>T	GRCh38
NC_000013.10:g.28498881C>T , CM000675.1:g.28498881C>T	GRCh37
NC_000013.9:g.27396881C>T	NCBI36
NG_008183.1:g.9714C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381033.5:c.*43C>T MANE Select	ENSP00000370421.4:n.*43C>T
ENST00000381033.4:c.*43C>T	ENSP00000370421.4:n.*43C>T
NM_000209.3:c.*43C>T	NP_000200.1:n.*43C>T
NM_000209.4:c.*43C>T MANE Select	NP_000200.1:n.*43C>T