Canonical Allele Identifier: CA15599262

Gene: GFI1B

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.132991261C>G , CM000671.2:g.132991261C>G	GRCh38
NC_000009.11:g.135866648C>G , CM000671.1:g.135866648C>G	GRCh37
NC_000009.10:g.134856469C>G	NCBI36
NG_034227.1:g.50717C>G , LRG_879:g.50717C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372122.4:c.*211C>G MANE Select	ENSP00000361195.1:n.*211C>G
ENST00000372123.5:c.*211C>G	ENSP00000361196.1:n.*211C>G
ENST00000636137.1:c.*211C>G	ENSP00000490303.1:n.*211C>G
ENST00000636263.1:c.1300C>G	ENSP00000489646.1:n.1300C>G
ENST00000339463.7:c.*211C>G	ENSP00000344782.3:n.*211C>G
ENST00000372122.3:c.*211C>G	ENSP00000361195.1:n.*211C>G
ENST00000372123.4:c.*211C>G	ENSP00000361196.1:n.*211C>G
NM_001135031.1:c.*211C>G	NP_001128503.1:n.*211C>G
NM_004188.5:c.*211C>G , LRG_879t1:c.*211C>G	NP_004179.3:n.*211C>G
XM_006717297.2:c.*211C>G	XP_006717360.1:n.*211C>G
XM_006717298.2:c.*211C>G	XP_006717361.1:n.*211C>G
XM_011519068.1:c.*211C>G	XP_011517370.1:n.*211C>G
XM_011519069.1:c.*211C>G	XP_011517371.1:n.*211C>G
XM_011519070.1:c.*211C>G	XP_011517372.1:n.*211C>G
XR_929847.1:n.1826C>G
NM_004188.6:c.*211C>G	NP_004179.3:n.*211C>G
XM_006717297.3:c.*211C>G	XP_006717360.1:n.*211C>G
XM_011519068.2:c.*211C>G	XP_011517370.1:n.*211C>G
XM_011519069.2:c.*211C>G	XP_011517371.1:n.*211C>G
XM_011519070.2:c.*211C>G	XP_011517372.1:n.*211C>G
XM_017015175.1:c.*211C>G	XP_016870664.1:n.*211C>G
XM_017015176.1:c.*211C>G	XP_016870665.1:n.*211C>G
NM_001135031.2:c.*211C>G	NP_001128503.1:n.*211C>G
NM_001371908.1:c.*211C>G	NP_001358837.1:n.*211C>G
NM_001377304.1:c.*211C>G MANE Select	NP_001364233.1:n.*211C>G
NM_001377305.1:c.*211C>G	NP_001364234.1:n.*211C>G
NM_004188.8:c.*211C>G	NP_004179.3:n.*211C>G