Canonical Allele Identifier: CA1554040952
Gene: SMN2 HGNC NCBI

Linked Data

dbSNP Id: rs1774423638

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.70049560_70049561del , CM000667.2:g.70049560_70049561del GRCh38
NC_000005.9:g.69345387_69345388del , CM000667.1:g.69345387_69345388del GRCh37
NC_000005.8:g.69381143_69381144del NCBI36
NG_008728.1:g.5038_5039del

Transcript Alleles

HGVS Amino-acid Change
NM_017411.3:c.-126_-125del NP_059107.1:n.-126_-125del
NM_022875.2:c.-126_-125del NP_075013.1:n.-126_-125del
NM_022876.2:c.-126_-125del NP_075014.1:n.-126_-125del
NM_022877.2:c.-126_-125del NP_075015.1:n.-126_-125del
XR_948432.1:n.1054+61556_1054+61557del