Canonical Allele Identifier: CA983969247

Gene: NAGS PYY

Linked Data

• dbSNP Id: rs2049090375
• gnomAD v3: 17-44006276-C-G
• gnomAD v4: 17-44006276-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44006276C>G , CM000679.2:g.44006276C>G	GRCh38
NC_000017.10:g.42083644C>G , CM000679.1:g.42083644C>G	GRCh37
NC_000017.9:g.39439170C>G	NCBI36
NG_008106.1:g.6613C>G
NG_023338.1:g.3194G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293404.8:c.915+39C>G (NAGS) MANE Select	ENSP00000293404.2:n.915+39C>G
ENST00000293404.7:c.915+39C>G (NAGS)	ENSP00000293404.2:n.915+39C>G
ENST00000589767.1:c.822+39C>G (NAGS)	ENSP00000465408.1:n.822+39C>G
ENST00000592915.1:n.190+39C>G (NAGS)
NM_153006.2:c.915+39C>G (NAGS)	NP_694551.1:n.915+39C>G
XM_011524438.1:c.915+39C>G (NAGS)	XP_011522740.1:n.915+39C>G
XM_011524439.1:c.417+39C>G (NAGS)	XP_011522741.1:n.417+39C>G
XM_011525035.1:c.-463+17296G>C (PYY)	XP_011523337.1:n.-463+17296G>C
XM_011524439.2:c.417+39C>G (NAGS)	XP_011522741.1:n.417+39C>G
NM_153006.3:c.915+39C>G (NAGS) MANE Select	NP_694551.1:n.915+39C>G