Canonical Allele Identifier: CA356875765
Gene: SGCB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52027982T>A , CM000666.2:g.52027982T>A GRCh38
NC_000004.11:g.52894148T>A , CM000666.1:g.52894148T>A GRCh37
NC_000004.10:g.52588905T>A NCBI36
NG_008891.1:g.15338A>T , LRG_204:g.15338A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000381431.10:c.739A>T MANE Select ENSP00000370839.6:p.Met247Leu
ENST00000381431.9:c.739A>T ENSP00000370839.5:p.Met247Leu
NM_000232.4:c.739A>T , LRG_204t1:c.739A>T NP_000223.1:p.Met247Leu
XM_006714049.2:c.442A>T XP_006714112.1:p.Met148Leu
XM_011534403.1:c.529A>T XP_011532705.1:p.Met177Leu
XM_011534404.1:c.442A>T XP_011532706.1:p.Met148Leu
NM_000232.5:c.739A>T MANE Select NP_000223.1:p.Met247Leu