Canonical Allele Identifier: CA885864950

Gene: TSHB

Linked Data

• dbSNP Id: rs1427985828
• gnomAD v3: 1-115033185-A-C
• gnomAD v4: 1-115033185-A-C
• MyVariant Identifiers: chr1:g.115575806A>C (hg19) ; chr1:g.115033185A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115033185A>C , CM000663.2:g.115033185A>C	GRCh38
NC_000001.10:g.115575806A>C , CM000663.1:g.115575806A>C	GRCh37
NC_000001.9:g.115377329A>C	NCBI36
NG_015891.1:g.8392A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256592.3:c.-1-177A>C MANE Select	ENSP00000256592.1:n.-1-177A>C
ENST00000256592.2:c.-1-177A>C	ENSP00000256592.1:n.-1-177A>C
NM_000549.4:c.-1-177A>C	NP_000540.2:n.-1-177A>C
NM_000549.5:c.-1-177A>C MANE Select	NP_000540.2:n.-1-177A>C