Canonical Allele Identifier: CA1077260059
Gene: SMN2 HGNC NCBI

Linked Data

dbSNP Id: rs1774427162
gnomAD v3: 5-70049634-C-T
gnomAD v4: 5-70049634-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.70049634C>T , CM000667.2:g.70049634C>T GRCh38
NC_000005.9:g.69345461C>T , CM000667.1:g.69345461C>T GRCh37
NC_000005.8:g.69381217C>T NCBI36
NG_008728.1:g.5112C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000380743.8:c.-52C>T ENSP00000370119.4:n.-52C>T
NM_017411.3:c.-52C>T NP_059107.1:n.-52C>T
NM_022875.2:c.-52C>T NP_075013.1:n.-52C>T
NM_022876.2:c.-52C>T NP_075014.1:n.-52C>T
NM_022877.2:c.-52C>T NP_075015.1:n.-52C>T
XM_011543602.1:c.-52C>T XP_011541904.1:n.-52C>T
XM_011543603.1:c.-52C>T XP_011541905.1:n.-52C>T
XR_948432.1:n.1054+61630C>T
XM_011543602.3:c.-52C>T XP_011541904.1:n.-52C>T
XM_011543603.3:c.-52C>T XP_011541905.1:n.-52C>T