Canonical Allele Identifier: CA1554040991
Gene: SMN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.70049634C= , CM000667.2:g.70049634C= GRCh38
NC_000005.9:g.69345461C= , CM000667.1:g.69345461C= GRCh37
NC_000005.8:g.69381217C= NCBI36
NG_008728.1:g.5112C=

Transcript Alleles

HGVS Amino-acid change
ENST00000380743.8:c.-52C= ENSP00000370119.4:n.-52C=
NM_017411.3:c.-52C= NP_059107.1:n.-52C=
NM_022875.2:c.-52C= NP_075013.1:n.-52C=
NM_022876.2:c.-52C= NP_075014.1:n.-52C=
NM_022877.2:c.-52C= NP_075015.1:n.-52C=
XM_011543602.1:c.-52C= XP_011541904.1:n.-52C=
XM_011543603.1:c.-52C= XP_011541905.1:n.-52C=
XR_948432.1:n.1054+61630C=
XM_011543602.3:c.-52C= XP_011541904.1:n.-52C=
XM_011543603.3:c.-52C= XP_011541905.1:n.-52C=