Canonical Allele Identifier: CA378891262

Gene: IFITM5

Linked Data

• dbSNP Id: rs1337287179
• gnomAD v2: 11-299490-T-G
• gnomAD v3: 11-299490-T-G
• gnomAD v4: 11-299490-T-G
• MyVariant Identifiers: chr11:g.299490T>G (hg19) ; chr11:g.299490T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.299490T>G , CM000673.2:g.299490T>G	GRCh38
NC_000011.9:g.299490T>G , CM000673.1:g.299490T>G	GRCh37
NC_000011.8:g.289490T>G	NCBI36
NG_032892.1:g.5037A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382614.2:c.1A>C MANE Select	ENSP00000372059.2:p.Met1Leu
NM_001025295.2:c.1A>C	NP_001020466.1:p.Met1Leu
NM_001025295.3:c.1A>C MANE Select	NP_001020466.1:p.Met1Leu