Canonical Allele Identifier: CA2670614825
Gene: SGCB HGNC NCBI

Linked Data

gnomAD v4: 4-52038360-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038360G>C , CM000666.2:g.52038360G>C GRCh38
NC_000004.11:g.52904526G>C , CM000666.1:g.52904526G>C GRCh37
NC_000004.10:g.52599283G>C NCBI36
NG_008891.1:g.4960C>G , LRG_204:g.4960C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.9:c.-101C>G ENSP00000370839.5:n.-101C>G