Canonical Allele Identifier: CA1554040983
Gene: SMN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.70049605C= , CM000667.2:g.70049605C= GRCh38
NC_000005.9:g.69345432C= , CM000667.1:g.69345432C= GRCh37
NC_000005.8:g.69381188C= NCBI36
NG_008728.1:g.5083C=

Transcript Alleles

HGVS Amino-acid change
NM_017411.3:c.-81C= NP_059107.1:n.-81C=
NM_022875.2:c.-81C= NP_075013.1:n.-81C=
NM_022876.2:c.-81C= NP_075014.1:n.-81C=
NM_022877.2:c.-81C= NP_075015.1:n.-81C=
XR_948432.1:n.1054+61601C=