Canonical Allele Identifier: CA2674141839
Gene: SMN2 HGNC NCBI

Linked Data

gnomAD v4: 5-70049557-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.70049557A>G , CM000667.2:g.70049557A>G GRCh38
NC_000005.9:g.69345384A>G , CM000667.1:g.69345384A>G GRCh37
NC_000005.8:g.69381140A>G NCBI36
NG_008728.1:g.5035A>G

Transcript Alleles

HGVS Amino-acid Change
NM_017411.3:c.-129A>G NP_059107.1:n.-129A>G
NM_022875.2:c.-129A>G NP_075013.1:n.-129A>G
NM_022876.2:c.-129A>G NP_075014.1:n.-129A>G
NM_022877.2:c.-129A>G NP_075015.1:n.-129A>G
XR_948432.1:n.1054+61553A>G