Canonical Allele Identifier: CA560269427
Gene: SMN2 HGNC NCBI

Linked Data

dbSNP Id: rs1283987336
gnomAD v2: 5-69345432-C-T
gnomAD v3: 5-70049605-C-T
gnomAD v4: 5-70049605-C-T

Genomic Alleles

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

Transcript Alleles

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