Canonical Allele Identifier: CA1190425198

Gene: TSHB

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115033411C= , CM000663.2:g.115033411C=	GRCh38
NC_000001.10:g.115576032C= , CM000663.1:g.115576032C=	GRCh37
NC_000001.9:g.115377555C=	NCBI36
NG_015891.1:g.8618C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256592.3:c.49C= MANE Select	ENSP00000256592.1:p.Gln17=
ENST00000256592.2:c.49C=	ENSP00000256592.1:p.Gln17=
ENST00000369517.1:c.49C=	ENSP00000358530.1:p.Gln17=
NM_000549.4:c.49C=	NP_000540.2:p.Gln17=
XM_011542065.1:c.49C=	XP_011540367.1:p.Gln17=
XM_011542065.2:c.49C=	XP_011540367.1:p.Gln17=
NM_000549.5:c.49C= MANE Select	NP_000540.2:p.Gln17=