Canonical Allele Identifier: CA460496852

Gene: STAR

Linked Data

• MyVariant Identifiers: chr8:g.38003519T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.38146001T>G , CM000670.2:g.38146001T>G	GRCh38
NC_000008.10:g.38003519T>G , CM000670.1:g.38003519T>G	GRCh37
NC_000008.9:g.38122676T>G	NCBI36
NG_011827.1:g.10082A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000276449.9:c.612A>C MANE Select	ENSP00000276449.3:p.Thr204=
ENST00000276449.8:c.612A>C	ENSP00000276449.3:p.Thr204=
ENST00000520114.1:n.1099A>C
ENST00000522050.1:c.548A>C
NM_000349.2:c.612A>C	NP_000340.2:p.Thr204=
XM_006716392.1:c.612A>C	XP_006716455.1:p.Thr204=
NM_000349.3:c.612A>C MANE Select	NP_000340.2:p.Thr204=