Canonical Allele Identifier: CA356875775
Gene: SGCB HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.52894153C>A (hg19) chr4:g.52027987C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52027987C>A , CM000666.2:g.52027987C>A GRCh38
NC_000004.11:g.52894153C>A , CM000666.1:g.52894153C>A GRCh37
NC_000004.10:g.52588910C>A NCBI36
NG_008891.1:g.15333G>T , LRG_204:g.15333G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000381431.10:c.734G>T MANE Select ENSP00000370839.6:p.Gly245Val
ENST00000381431.9:c.734G>T ENSP00000370839.5:p.Gly245Val
NM_000232.4:c.734G>T , LRG_204t1:c.734G>T NP_000223.1:p.Gly245Val
XM_006714049.2:c.437G>T XP_006714112.1:p.Gly146Val
XM_011534403.1:c.524G>T XP_011532705.1:p.Gly175Val
XM_011534404.1:c.437G>T XP_011532706.1:p.Gly146Val
NM_000232.5:c.734G>T MANE Select NP_000223.1:p.Gly245Val
Search 100 bp 5'
Search 100 bp 3'