Canonical Allele Identifier: CA813569945
Gene: SMN2 HGNC NCBI

Linked Data

dbSNP Id: rs1276380162
gnomAD v3: 5-70049591-C-G
gnomAD v4: 5-70049591-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.70049591C>G , CM000667.2:g.70049591C>G GRCh38
NC_000005.9:g.69345418C>G , CM000667.1:g.69345418C>G GRCh37
NC_000005.8:g.69381174C>G NCBI36
NG_008728.1:g.5069C>G

Transcript Alleles

HGVS Amino-acid change
NM_017411.3:c.-95C>G NP_059107.1:n.-95C>G
NM_022875.2:c.-95C>G NP_075013.1:n.-95C>G
NM_022876.2:c.-95C>G NP_075014.1:n.-95C>G
NM_022877.2:c.-95C>G NP_075015.1:n.-95C>G
XR_948432.1:n.1054+61587C>G