Canonical Allele Identifier: CA2670614666

Gene: SGCB

Linked Data

• gnomAD v4: 4-52038274-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52038274C>A , CM000666.2:g.52038274C>A	GRCh38
NC_000004.11:g.52904440C>A , CM000666.1:g.52904440C>A	GRCh37
NC_000004.10:g.52599197C>A	NCBI36
NG_008891.1:g.5046G>T , LRG_204:g.5046G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381431.10:c.-15G>T MANE Select	ENSP00000370839.6:n.-15G>T
ENST00000381431.9:c.-15G>T	ENSP00000370839.5:n.-15G>T
NM_000232.4:c.-15G>T , LRG_204t1:c.-15G>T	NP_000223.1:n.-15G>T
XM_011534403.1:c.-15G>T	XP_011532705.1:n.-15G>T
NM_000232.5:c.-15G>T MANE Select	NP_000223.1:n.-15G>T