Canonical Allele Identifier: CA1555784452

Gene: GFM2 HEXB

Linked Data

• dbSNP Id: rs1749907805

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.74721940G>C , CM000667.2:g.74721940G>C	GRCh38
NC_000005.9:g.74017765G>C , CM000667.1:g.74017765G>C	GRCh37
NC_000005.8:g.74053521G>C	NCBI36
NG_009770.1:g.41797G>C
NG_011531.1:g.50278C>G
NG_009770.2:g.86918G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296805.8:c.2212-157C>G (GFM2) MANE Select	ENSP00000296805.3:n.2212-157C>G
ENST00000296805.7:c.2212-157C>G (GFM2)	ENSP00000296805.3:n.2212-157C>G
ENST00000345239.6:c.2071-157C>G (GFM2)	ENSP00000296804.3:n.2071-157C>G
ENST00000503312.5:c.608+504G>C (HEXB)
ENST00000505859.1:c.256-359G>C (HEXB)
ENST00000509430.5:c.2212-157C>G (GFM2)	ENSP00000427004.1:n.2212-157C>G
ENST00000513867.1:n.381-359G>C (HEXB)
ENST00000515125.5:n.615-157C>G (GFM2)
NM_001281302.1:c.2308-157C>G (GFM2)	NP_001268231.1:n.2308-157C>G
NM_032380.4:c.2212-157C>G (GFM2)	NP_115756.2:n.2212-157C>G
NM_170691.2:c.2071-157C>G (GFM2)	NP_733792.1:n.2071-157C>G
NR_104006.1:n.2531-157C>G (GFM2)
XM_006714721.2:c.2077-157C>G (GFM2)	XP_006714784.1:n.2077-157C>G
XM_011543690.1:c.2212-157C>G (GFM2)	XP_011541992.1:n.2212-157C>G
XM_017009986.1:c.2212-157C>G (GFM2)	XP_016865475.1:n.2212-157C>G
XR_002956185.1:n.3498-157C>G (GFM2)
NM_032380.5:c.2212-157C>G (GFM2) MANE Select	NP_115756.2:n.2212-157C>G
NM_001281302.2:c.2308-157C>G (GFM2)	NP_001268231.1:n.2308-157C>G
NM_170691.3:c.2071-157C>G (GFM2)	NP_733792.1:n.2071-157C>G
NR_104006.2:n.2277-157C>G (GFM2)