Canonical Allele Identifier: CA2686931500
Gene: STAR HGNC NCBI

Linked Data

gnomAD v4: 8-38144232-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38144232A>G , CM000670.2:g.38144232A>G GRCh38
NC_000008.10:g.38001750A>G , CM000670.1:g.38001750A>G GRCh37
NC_000008.9:g.38120907A>G NCBI36
NG_011827.1:g.11851T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000276449.9:c.*41T>C MANE Select ENSP00000276449.3:n.*41T>C
ENST00000276449.8:c.*41T>C ENSP00000276449.3:n.*41T>C
ENST00000520114.1:n.2868T>C
ENST00000522050.1:c.741T>C
NM_000349.2:c.*41T>C NP_000340.2:n.*41T>C
XM_006716392.1:c.805T>C XP_006716455.1:p.Tyr269His
NM_000349.3:c.*41T>C MANE Select NP_000340.2:n.*41T>C