Canonical Allele Identifier: CA1554040990
Gene: SMN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.70049623G= , CM000667.2:g.70049623G= GRCh38
NC_000005.9:g.69345450G= , CM000667.1:g.69345450G= GRCh37
NC_000005.8:g.69381206G= NCBI36
NG_008728.1:g.5101G=

Transcript Alleles

HGVS Amino-acid change
ENST00000380743.8:c.-63G= ENSP00000370119.4:n.-63G=
NM_017411.3:c.-63G= NP_059107.1:n.-63G=
NM_022875.2:c.-63G= NP_075013.1:n.-63G=
NM_022876.2:c.-63G= NP_075014.1:n.-63G=
NM_022877.2:c.-63G= NP_075015.1:n.-63G=
XR_948432.1:n.1054+61619G=