Canonical Allele Identifier: CA356875761
Gene: SGCB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52027980C>T , CM000666.2:g.52027980C>T GRCh38
NC_000004.11:g.52894146C>T , CM000666.1:g.52894146C>T GRCh37
NC_000004.10:g.52588903C>T NCBI36
NG_008891.1:g.15340G>A , LRG_204:g.15340G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000381431.10:c.741G>A MANE Select ENSP00000370839.6:p.Met247Ile
ENST00000381431.9:c.741G>A ENSP00000370839.5:p.Met247Ile
NM_000232.4:c.741G>A , LRG_204t1:c.741G>A NP_000223.1:p.Met247Ile
XM_006714049.2:c.444G>A XP_006714112.1:p.Met148Ile
XM_011534403.1:c.531G>A XP_011532705.1:p.Met177Ile
XM_011534404.1:c.444G>A XP_011532706.1:p.Met148Ile
NM_000232.5:c.741G>A MANE Select NP_000223.1:p.Met247Ile