Canonical Allele Identifier: CA2709254683
Gene: SMN2 HGNC NCBI

Linked Data

dbSNP Id: rs2112463605

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.70049573_70049575del , CM000667.2:g.70049573_70049575del GRCh38
NC_000005.9:g.69345400_69345402del , CM000667.1:g.69345400_69345402del GRCh37
NC_000005.8:g.69381156_69381158del NCBI36
NG_008728.1:g.5051_5053del

Transcript Alleles

HGVS Amino-acid Change
NM_017411.3:c.-113_-111del NP_059107.1:n.-113_-111del
NM_022875.2:c.-113_-111del NP_075013.1:n.-113_-111del
NM_022876.2:c.-113_-111del NP_075014.1:n.-113_-111del
NM_022877.2:c.-113_-111del NP_075015.1:n.-113_-111del
XR_948432.1:n.1054+61569_1054+61571del