Canonical Allele Identifier: CA133979609

Linked Data

dbSNP Id: rs959790388
gnomAD v3: 6-7541626-T-G
gnomAD v4: 6-7541626-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7541626T>G , CM000668.2:g.7541626T>G GRCh38
NC_000006.11:g.7541859T>G , CM000668.1:g.7541859T>G GRCh37
NC_000006.10:g.7486858T>G NCBI36
NG_008803.1:g.4990T>G , LRG_423:g.4990T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000710359.1:c.-290T>G (DSP) ENSP00000518230.1:n.-290T>G
ENST00000379802.7:c.-290T>G (DSP) ENSP00000369129.3:n.-290T>G
ENST00000418664.2:c.-290T>G (DSP) ENSP00000396591.2:n.-290T>G
XM_011514323.1:c.-290T>G (DSP) XP_011512625.1:n.-290T>G
XR_241971.2:n.269-573A>C (DSP-AS1)
NM_001008844.2:c.-290T>G (DSP) NP_001008844.1:n.-290T>G
NM_001319034.1:c.-290T>G (DSP) NP_001305963.1:n.-290T>G
NM_004415.3:c.-290T>G (DSP) NP_004406.2:n.-290T>G
XR_241970.4:n.101A>C (DSP-AS1)
XR_241971.3:n.270-573A>C (DSP-AS1)