Canonical Allele Identifier: CA2670614758
Gene: SGCB HGNC NCBI

Linked Data

gnomAD v4: 4-52038324-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038324T>G , CM000666.2:g.52038324T>G GRCh38
NC_000004.11:g.52904490T>G , CM000666.1:g.52904490T>G GRCh37
NC_000004.10:g.52599247T>G NCBI36
NG_008891.1:g.4996A>C , LRG_204:g.4996A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.9:c.-65A>C ENSP00000370839.5:n.-65A>C