Canonical Allele Identifier: CA2766889319
Gene: SMN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.70049587C>G , CM000667.2:g.70049587C>G GRCh38
NC_000005.9:g.69345414C>G , CM000667.1:g.69345414C>G GRCh37
NC_000005.8:g.69381170C>G NCBI36
NG_008728.1:g.5065C>G

Transcript Alleles

HGVS Amino-acid Change
NM_017411.3:c.-99C>G NP_059107.1:n.-99C>G
NM_022875.2:c.-99C>G NP_075013.1:n.-99C>G
NM_022876.2:c.-99C>G NP_075014.1:n.-99C>G
NM_022877.2:c.-99C>G NP_075015.1:n.-99C>G
XR_948432.1:n.1054+61583C>G