Canonical Allele Identifier: CA372779354
Community Standard Title: NM_003070.5(SMARCA2):c.196C>G (p.Pro66Ala)
Gene: SMARCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2029218C>G , CM000671.2:g.2029218C>G GRCh38
NC_000009.11:g.2029218C>G , CM000671.1:g.2029218C>G GRCh37
NC_000009.10:g.2019218C>G NCBI36
NG_032162.1:g.18877C>G
NG_032162.2:g.53929C>G

Transcript Alleles

HGVS Amino-acid Change
NM_003070.5:c.196C>G MANE Select NP_003061.3:p.Pro66Ala
ENST00000349721.8:c.196C>G MANE Select ENSP00000265773.5:p.Pro66Ala
NM_001289396.1:c.196C>G NP_001276325.1:p.Pro66Ala
NM_001289397.1:c.196C>G NP_001276326.1:p.Pro66Ala
NM_001289397.2:c.196C>G NP_001276326.1:p.Pro66Ala
NM_003070.4:c.196C>G NP_003061.3:p.Pro66Ala
NM_139045.3:c.196C>G NP_620614.2:p.Pro66Ala
NM_139045.4:c.196C>G NP_620614.2:p.Pro66Ala
ENST00000349721.7:c.196C>G ENSP00000265773.5:p.Pro66Ala
ENST00000357248.7:c.196C>G ENSP00000349788.2:p.Pro66Ala
ENST00000357248.8:c.196C>G ENSP00000349788.2:p.Pro66Ala
ENST00000382194.6:c.196C>G ENSP00000371629.1:p.Pro66Ala
ENST00000382203.5:c.196C>G ENSP00000371638.1:p.Pro66Ala
ENST00000439732.6:c.196C>G ENSP00000409398.2:p.Pro66Ala
ENST00000450198.6:c.196C>G ENSP00000392081.2:p.Pro66Ala
ENST00000457226.2:c.196C>G ENSP00000415218.2:p.Pro66Ala
ENST00000634287.1:c.-54-3734C>G ENSP00000489142.1:n.-54-3734C>G
ENST00000634536.1:n.290C>G
ENST00000634760.1:c.196C>G ENSP00000489256.1:p.Pro66Ala
ENST00000636559.1:c.196C>G ENSP00000490852.1:p.Pro66Ala
ENST00000636903.1:c.196C>G ENSP00000489968.1:p.Pro66Ala
ENST00000637103.1:c.196C>G ENSP00000490486.1:p.Pro66Ala
ENST00000637134.2:c.196C>G ENSP00000489667.2:p.Pro66Ala
ENST00000637806.1:c.196C>G ENSP00000490551.1:p.Pro66Ala
ENST00000704350.1:c.-5-10248C>G ENSP00000515861.1:n.-5-10248C>G
ENST00000704351.1:c.196C>G ENSP00000515862.1:p.Pro66Ala
ENST00000704352.1:c.196C>G ENSP00000515863.1:p.Pro66Ala
ENST00000704353.1:c.196C>G ENSP00000515864.1:p.Pro66Ala