Canonical Allele Identifier: CA2520210233
Gene: SGCB HGNC NCBI

Linked Data

gnomAD v4: 4-52038076-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038076T>G , CM000666.2:g.52038076T>G GRCh38
NC_000004.11:g.52904242T>G , CM000666.1:g.52904242T>G GRCh37
NC_000004.10:g.52598999T>G NCBI36
NG_008891.1:g.5244A>C , LRG_204:g.5244A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.10:c.33+151A>C MANE Select ENSP00000370839.6:n.33+151A>C
ENST00000381431.9:c.33+151A>C ENSP00000370839.5:n.33+151A>C
ENST00000506357.5:c.19+151A>C
NM_000232.4:c.33+151A>C , LRG_204t1:c.33+151A>C NP_000223.1:n.33+151A>C
XM_011534403.1:c.33+151A>C XP_011532705.1:n.33+151A>C
NM_000232.5:c.33+151A>C MANE Select NP_000223.1:n.33+151A>C
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