Canonical Allele Identifier: CA983969043

Linked Data

dbSNP Id: rs2049083857

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44005980C>T , CM000679.2:g.44005980C>T GRCh38
NC_000017.10:g.42083348C>T , CM000679.1:g.42083348C>T GRCh37
NC_000017.9:g.39438874C>T NCBI36
NG_008106.1:g.6317C>T
NG_023338.1:g.3490G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000293404.8:c.702-44C>T (NAGS) MANE Select ENSP00000293404.2:n.702-44C>T
ENST00000293404.7:c.702-44C>T (NAGS) ENSP00000293404.2:n.702-44C>T
ENST00000589767.1:c.609-44C>T (NAGS) ENSP00000465408.1:n.609-44C>T
NM_153006.2:c.702-44C>T (NAGS) NP_694551.1:n.702-44C>T
XM_011524438.1:c.702-44C>T (NAGS) XP_011522740.1:n.702-44C>T
XM_011524439.1:c.204-44C>T (NAGS) XP_011522741.1:n.204-44C>T
XM_011525035.1:c.-463+17592G>A (PYY) XP_011523337.1:n.-463+17592G>A
XM_011524439.2:c.204-44C>T (NAGS) XP_011522741.1:n.204-44C>T
NM_153006.3:c.702-44C>T (NAGS) MANE Select NP_694551.1:n.702-44C>T