Canonical Allele Identifier: CA1457434216
Gene: SGCB HGNC NCBI

Linked Data

dbSNP Id: rs1057521583
gnomAD v4: 4-52038278-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038278G>A , CM000666.2:g.52038278G>A GRCh38
NC_000004.11:g.52904444G>A , CM000666.1:g.52904444G>A GRCh37
NC_000004.10:g.52599201G>A NCBI36
NG_008891.1:g.5042C>T , LRG_204:g.5042C>T

Transcript Alleles

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