Canonical Allele Identifier: CA2670614661
Gene: SGCB HGNC NCBI

Linked Data

gnomAD v4: 4-52038272-G-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038272G>T , CM000666.2:g.52038272G>T GRCh38
NC_000004.11:g.52904438G>T , CM000666.1:g.52904438G>T GRCh37
NC_000004.10:g.52599195G>T NCBI36
NG_008891.1:g.5048C>A , LRG_204:g.5048C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.10:c.-13C>A MANE Select ENSP00000370839.6:n.-13C>A
ENST00000381431.9:c.-13C>A ENSP00000370839.5:n.-13C>A
NM_000232.4:c.-13C>A , LRG_204t1:c.-13C>A NP_000223.1:n.-13C>A
XM_011534403.1:c.-13C>A XP_011532705.1:n.-13C>A
NM_000232.5:c.-13C>A MANE Select NP_000223.1:n.-13C>A
Search 100 bp 5'
Search 100 bp 3'