Canonical Allele Identifier: CA433784545

Gene: STAB1

Linked Data

• gnomAD v4: 3-52506766-C-T
• MyVariant Identifiers: chr3:g.52540782C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52506766C>T , CM000665.2:g.52506766C>T	GRCh38
NC_000003.11:g.52540782C>T , CM000665.1:g.52540782C>T	GRCh37
NC_000003.10:g.52515822C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000321725.10:c.1905C>T MANE Select	ENSP00000312946.6:p.His635=
ENST00000481607.1:n.1960C>T
NM_015136.2:c.1905C>T	NP_055951.2:p.His635=
XM_005264973.2:c.1905C>T	XP_005265030.1:p.His635=
XM_005264974.2:c.1905C>T	XP_005265031.1:p.His635=
XM_005264975.2:c.1905C>T	XP_005265032.1:p.His635=
XM_006713065.1:c.1905C>T	XP_006713128.1:p.His635=
XM_011533528.1:c.1905C>T	XP_011531830.1:p.His635=
XR_940395.1:n.1981C>T
XM_005264973.3:c.1905C>T	XP_005265030.1:p.His635=
XM_017005998.1:c.1905C>T	XP_016861487.1:p.His635=
XM_017005999.1:c.1905C>T	XP_016861488.1:p.His635=
XM_017006000.1:c.1905C>T	XP_016861489.1:p.His635=
XM_017006001.1:c.1905C>T	XP_016861490.1:p.His635=
XM_017006002.1:c.1905C>T	XP_016861491.1:p.His635=
XM_017006003.1:c.1905C>T	XP_016861492.1:p.His635=
XM_017006004.2:c.1905C>T	XP_016861493.1:p.His635=
XR_001740064.1:n.1981C>T
NM_015136.3:c.1905C>T MANE Select	NP_055951.2:p.His635=