Canonical Allele Identifier: CA1077259951
Gene: SMN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.70049537G>C , CM000667.2:g.70049537G>C GRCh38
NC_000005.9:g.69345364G>C , CM000667.1:g.69345364G>C GRCh37
NC_000005.8:g.69381120G>C NCBI36
NG_008728.1:g.5015G>C

Transcript Alleles

HGVS Amino-acid Change
NM_017411.3:c.-149G>C NP_059107.1:n.-149G>C
NM_022875.2:c.-149G>C NP_075013.1:n.-149G>C
NM_022876.2:c.-149G>C NP_075014.1:n.-149G>C
NM_022877.2:c.-149G>C NP_075015.1:n.-149G>C
XR_948432.1:n.1054+61533G>C