Canonical Allele Identifier: CA2578086607
Gene: SGCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52027943C>T , CM000666.2:g.52027943C>T GRCh38
NC_000004.11:g.52894109C>T , CM000666.1:g.52894109C>T GRCh37
NC_000004.10:g.52588866C>T NCBI36
NG_008891.1:g.15377G>A , LRG_204:g.15377G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000381431.10:c.753+25G>A MANE Select ENSP00000370839.6:n.753+25G>A
ENST00000381431.9:c.753+25G>A ENSP00000370839.5:n.753+25G>A
NM_000232.4:c.753+25G>A , LRG_204t1:c.753+25G>A NP_000223.1:n.753+25G>A
XM_006714049.2:c.456+25G>A XP_006714112.1:n.456+25G>A
XM_011534403.1:c.543+25G>A XP_011532705.1:n.543+25G>A
XM_011534404.1:c.456+25G>A XP_011532706.1:n.456+25G>A
NM_000232.5:c.753+25G>A MANE Select NP_000223.1:n.753+25G>A