Canonical Allele Identifier: CA2766889317
Gene: SMN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.70049569T>G , CM000667.2:g.70049569T>G GRCh38
NC_000005.9:g.69345396T>G , CM000667.1:g.69345396T>G GRCh37
NC_000005.8:g.69381152T>G NCBI36
NG_008728.1:g.5047T>G

Transcript Alleles

HGVS Amino-acid Change
NM_017411.3:c.-117T>G NP_059107.1:n.-117T>G
NM_022875.2:c.-117T>G NP_075013.1:n.-117T>G
NM_022876.2:c.-117T>G NP_075014.1:n.-117T>G
NM_022877.2:c.-117T>G NP_075015.1:n.-117T>G
XR_948432.1:n.1054+61565T>G