Canonical Allele Identifier: CA356875794
Gene: SGCB HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.52894161G>T (hg19) chr4:g.52027995G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52027995G>T , CM000666.2:g.52027995G>T GRCh38
NC_000004.11:g.52894161G>T , CM000666.1:g.52894161G>T GRCh37
NC_000004.10:g.52588918G>T NCBI36
NG_008891.1:g.15325C>A , LRG_204:g.15325C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.10:c.726C>A MANE Select ENSP00000370839.6:p.His242Gln
ENST00000381431.9:c.726C>A ENSP00000370839.5:p.His242Gln
NM_000232.4:c.726C>A , LRG_204t1:c.726C>A NP_000223.1:p.His242Gln
XM_006714049.2:c.429C>A XP_006714112.1:p.His143Gln
XM_011534403.1:c.516C>A XP_011532705.1:p.His172Gln
XM_011534404.1:c.429C>A XP_011532706.1:p.His143Gln
NM_000232.5:c.726C>A MANE Select NP_000223.1:p.His242Gln
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