Canonical Allele Identifier: CA813569947
Gene: SMN2 HGNC NCBI

Linked Data

dbSNP Id: rs1229568194
gnomAD v3: 5-70049600-T-G
gnomAD v4: 5-70049600-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.70049600T>G , CM000667.2:g.70049600T>G GRCh38
NC_000005.9:g.69345427T>G , CM000667.1:g.69345427T>G GRCh37
NC_000005.8:g.69381183T>G NCBI36
NG_008728.1:g.5078T>G

Transcript Alleles

HGVS Amino-acid change
NM_017411.3:c.-86T>G NP_059107.1:n.-86T>G
NM_022875.2:c.-86T>G NP_075013.1:n.-86T>G
NM_022876.2:c.-86T>G NP_075014.1:n.-86T>G
NM_022877.2:c.-86T>G NP_075015.1:n.-86T>G
XR_948432.1:n.1054+61596T>G