Canonical Allele Identifier: CA674605145

Gene: TH

Linked Data

• dbSNP Id: rs1236937998
• gnomAD v4: 11-2171942-GA-G
• MyVariant Identifiers: chr11:g.2193173del (hg19) ; chr11:g.2171943del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2171943del , CM000673.2:g.2171943del	GRCh38
NC_000011.9:g.2193173del , CM000673.1:g.2193173del	GRCh37
NC_000011.8:g.2149749del	NCBI36
NG_008128.1:g.4863del

Transcript Alleles

HGVS	Amino-acid Change
XM_011520335.1:c.-157del	XP_011518637.1:n.-157del
XM_011520335.2:c.-157del	XP_011518637.1:n.-157del