Canonical Allele Identifier: CA1457434138

Gene: SGCB

Linked Data

• dbSNP Id: rs1737450226
• gnomAD v4: 4-52038181-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52038181G>A , CM000666.2:g.52038181G>A	GRCh38
NC_000004.11:g.52904347G>A , CM000666.1:g.52904347G>A	GRCh37
NC_000004.10:g.52599104G>A	NCBI36
NG_008891.1:g.5139C>T , LRG_204:g.5139C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381431.10:c.33+46C>T MANE Select	ENSP00000370839.6:n.33+46C>T
ENST00000381431.9:c.33+46C>T	ENSP00000370839.5:n.33+46C>T
ENST00000506357.5:c.19+46C>T
NM_000232.4:c.33+46C>T , LRG_204t1:c.33+46C>T	NP_000223.1:n.33+46C>T
XM_011534403.1:c.33+46C>T	XP_011532705.1:n.33+46C>T
NM_000232.5:c.33+46C>T MANE Select	NP_000223.1:n.33+46C>T