Canonical Allele Identifier: CA439273624
Gene: SGCB HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.52894155A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52027989A>C , CM000666.2:g.52027989A>C GRCh38
NC_000004.11:g.52894155A>C , CM000666.1:g.52894155A>C GRCh37
NC_000004.10:g.52588912A>C NCBI36
NG_008891.1:g.15331T>G , LRG_204:g.15331T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000381431.10:c.732T>G MANE Select ENSP00000370839.6:p.Gly244=
ENST00000381431.9:c.732T>G ENSP00000370839.5:p.Gly244=
NM_000232.4:c.732T>G , LRG_204t1:c.732T>G NP_000223.1:p.Gly244=
XM_006714049.2:c.435T>G XP_006714112.1:p.Gly145=
XM_011534403.1:c.522T>G XP_011532705.1:p.Gly174=
XM_011534404.1:c.435T>G XP_011532706.1:p.Gly145=
NM_000232.5:c.732T>G MANE Select NP_000223.1:p.Gly244=
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