Canonical Allele Identifier: CA2670598637
Gene: SGCB HGNC NCBI

Linked Data

gnomAD v4: 4-52028108-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52028108T>C , CM000666.2:g.52028108T>C GRCh38
NC_000004.11:g.52894274T>C , CM000666.1:g.52894274T>C GRCh37
NC_000004.10:g.52589031T>C NCBI36
NG_008891.1:g.15212A>G , LRG_204:g.15212A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.10:c.622-9A>G MANE Select ENSP00000370839.6:n.622-9A>G
ENST00000381431.9:c.622-9A>G ENSP00000370839.5:n.622-9A>G
NM_000232.4:c.622-9A>G , LRG_204t1:c.622-9A>G NP_000223.1:n.622-9A>G
XM_006714049.2:c.325-9A>G XP_006714112.1:n.325-9A>G
XM_011534403.1:c.412-9A>G XP_011532705.1:n.412-9A>G
XM_011534404.1:c.325-9A>G XP_011532706.1:n.325-9A>G
NM_000232.5:c.622-9A>G MANE Select NP_000223.1:n.622-9A>G