Canonical Allele Identifier: CA1457434233
Gene: SGCB HGNC NCBI

Linked Data

dbSNP Id: rs1737459058
gnomAD v4: 4-52038298-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038298G>A , CM000666.2:g.52038298G>A GRCh38
NC_000004.11:g.52904464G>A , CM000666.1:g.52904464G>A GRCh37
NC_000004.10:g.52599221G>A NCBI36
NG_008891.1:g.5022C>T , LRG_204:g.5022C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.10:c.-39C>T MANE Select ENSP00000370839.6:n.-39C>T
ENST00000381431.9:c.-39C>T ENSP00000370839.5:n.-39C>T
NM_000232.4:c.-39C>T , LRG_204t1:c.-39C>T NP_000223.1:n.-39C>T
XM_011534403.1:c.-39C>T XP_011532705.1:n.-39C>T
NM_000232.5:c.-39C>T MANE Select NP_000223.1:n.-39C>T