Canonical Allele Identifier: CA2683134189

Linked Data

gnomAD v4: 7-66995193-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.66995193C>T , CM000669.2:g.66995193C>T GRCh38
NC_000007.13:g.66460180C>T , CM000669.1:g.66460180C>T GRCh37
NC_000007.12:g.66097615C>T NCBI36
NG_007277.1:g.5409G>A , LRG_104:g.5409G>A
NG_033069.1:g.3389C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000414306.6:c.128+97G>A (SBDS) ENSP00000394586.1:n.128+97G>A
ENST00000697861.1:c.128+97G>A (SBDS) ENSP00000513460.1:n.128+97G>A
ENST00000697862.1:c.128+97G>A (SBDS) ENSP00000513461.1:n.128+97G>A
ENST00000697863.1:c.71+97G>A (SBDS) ENSP00000513462.1:n.71+97G>A
ENST00000697864.1:n.421G>A (SBDS)
ENST00000697865.1:c.71+97G>A (SBDS) ENSP00000513463.1:n.71+97G>A
ENST00000697866.1:c.-286G>A (SBDS) ENSP00000513464.1:n.-286G>A
ENST00000697868.1:c.128+97G>A (SBDS) ENSP00000513466.1:n.128+97G>A
ENST00000697869.1:c.128+97G>A (SBDS) ENSP00000513467.1:n.128+97G>A
ENST00000697897.1:c.128+97G>A (SBDS) ENSP00000513469.1:n.128+97G>A
ENST00000246868.7:c.128+97G>A (SBDS) MANE Select ENSP00000246868.2:n.128+97G>A
ENST00000246868.6:c.128+97G>A (SBDS) ENSP00000246868.2:n.128+97G>A
ENST00000414306.5:c.128+97G>A (SBDS) ENSP00000394586.1:n.128+97G>A
ENST00000490953.5:n.277+97G>A (SBDS)
ENST00000491969.5:n.21C>T (TYW1)
ENST00000617799.1:c.127+97G>A (SBDS) ENSP00000483040.1:n.127+97G>A
NM_016038.2:c.128+97G>A , LRG_104t1:c.128+97G>A (SBDS) NP_057122.2:n.128+97G>A
NM_016038.3:c.128+97G>A (SBDS) NP_057122.2:n.128+97G>A
NM_016038.4:c.128+97G>A (SBDS) MANE Select NP_057122.2:n.128+97G>A