Canonical Allele Identifier: CA378892721

Gene: IFITM2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.308315G>T , CM000673.2:g.308315G>T	GRCh38
NC_000011.9:g.308315G>T , CM000673.1:g.308315G>T	GRCh37
NC_000011.8:g.298315G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_006435.3:c.123G>T MANE Select	NP_006426.2:p.Met41Ile
ENST00000616316.3:c.123G>T MANE Select	ENSP00000484689.1:p.Met41Ile
NM_006435.2:c.123G>T	NP_006426.2:p.Met41Ile
ENST00000399817.8:c.123G>T	ENSP00000382714.4:p.Met41Ile
ENST00000399817.9:c.123G>T	ENSP00000382714.5:p.Met41Ile
ENST00000533141.1:c.63G>T	ENSP00000434443.1:p.Met21Ile
ENST00000602569.1:c.63G>T	ENSP00000473587.1:p.Met21Ile
ENST00000602569.2:c.63G>T	ENSP00000473587.2:p.Met21Ile
ENST00000616316.1:c.123G>T	ENSP00000484689.1:p.Met41Ile
ENST00000616316.2:c.123G>T	ENSP00000484689.1:p.Met41Ile
ENST00000679962.1:c.63G>T	ENSP00000505869.1:p.Met21Ile
ENST00000680011.1:n.123G>T
ENST00000680081.1:c.63G>T	ENSP00000505487.1:p.Met21Ile
ENST00000680197.1:c.123G>T	ENSP00000505840.1:p.Met41Ile
ENST00000680261.1:c.123G>T	ENSP00000506427.1:p.Met41Ile
ENST00000680344.1:c.123G>T	ENSP00000506171.1:p.Met41Ile
ENST00000680619.1:c.123G>T	ENSP00000504960.1:p.Met41Ile
ENST00000681276.1:c.63G>T	ENSP00000506694.1:p.Met21Ile
ENST00000681810.1:c.63G>T	ENSP00000505185.1:p.Met21Ile
ENST00000681833.1:c.123G>T	ENSP00000505420.1:p.Met41Ile
ENST00000681900.1:c.63G>T	ENSP00000506549.1:p.Met21Ile
ENST00000681914.1:c.63G>T	ENSP00000505868.1:p.Met21Ile