Canonical Allele Identifier: CA1777411929
Gene: STAR HGNC NCBI

Linked Data

dbSNP Id: rs1802583096

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38146844G>A , CM000670.2:g.38146844G>A GRCh38
NC_000008.10:g.38004362G>A , CM000670.1:g.38004362G>A GRCh37
NC_000008.9:g.38123519G>A NCBI36
NG_011827.1:g.9239C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000276449.9:c.307-397C>T MANE Select ENSP00000276449.3:n.307-397C>T
ENST00000276449.8:c.307-397C>T ENSP00000276449.3:n.307-397C>T
ENST00000520114.1:n.794-397C>T
ENST00000521236.1:c.61-397C>T ENSP00000430030.1:n.61-397C>T
ENST00000522050.1:c.243-397C>T
NM_000349.2:c.307-397C>T NP_000340.2:n.307-397C>T
XM_006716392.1:c.307-397C>T XP_006716455.1:n.307-397C>T
NM_000349.3:c.307-397C>T MANE Select NP_000340.2:n.307-397C>T