Canonical Allele Identifier: CA2674141842
Gene: SMN2 HGNC NCBI

Linked Data

gnomAD v4: 5-70049596-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.70049596G>C , CM000667.2:g.70049596G>C GRCh38
NC_000005.9:g.69345423G>C , CM000667.1:g.69345423G>C GRCh37
NC_000005.8:g.69381179G>C NCBI36
NG_008728.1:g.5074G>C

Transcript Alleles

HGVS Amino-acid Change
NM_017411.3:c.-90G>C NP_059107.1:n.-90G>C
NM_022875.2:c.-90G>C NP_075013.1:n.-90G>C
NM_022876.2:c.-90G>C NP_075014.1:n.-90G>C
NM_022877.2:c.-90G>C NP_075015.1:n.-90G>C
XR_948432.1:n.1054+61592G>C