Canonical Allele Identifier: CA2670598940
Gene: SGCB HGNC NCBI

Linked Data

gnomAD v4: 4-52028698-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52028698C>A , CM000666.2:g.52028698C>A GRCh38
NC_000004.11:g.52894864C>A , CM000666.1:g.52894864C>A GRCh37
NC_000004.10:g.52589621C>A NCBI36
NG_008891.1:g.14622G>T , LRG_204:g.14622G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.10:c.621+32G>T MANE Select ENSP00000370839.6:n.621+32G>T
ENST00000381431.9:c.621+32G>T ENSP00000370839.5:n.621+32G>T
NM_000232.4:c.621+32G>T , LRG_204t1:c.621+32G>T NP_000223.1:n.621+32G>T
XM_006714049.2:c.324+32G>T XP_006714112.1:n.324+32G>T
XM_011534403.1:c.411+32G>T XP_011532705.1:n.411+32G>T
XM_011534404.1:c.324+32G>T XP_011532706.1:n.324+32G>T
NM_000232.5:c.621+32G>T MANE Select NP_000223.1:n.621+32G>T