Canonical Allele Identifier: CA378891001

Gene: IFITM5

Linked Data

• gnomAD v4: 11-299420-A-G
• MyVariant Identifiers: chr11:g.299420A>G (hg19) ; chr11:g.299420A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.299420A>G , CM000673.2:g.299420A>G	GRCh38
NC_000011.9:g.299420A>G , CM000673.1:g.299420A>G	GRCh37
NC_000011.8:g.289420A>G	NCBI36
NG_032892.1:g.5107T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382614.2:c.71T>C MANE Select	ENSP00000372059.2:p.Leu24Pro
NM_001025295.2:c.71T>C	NP_001020466.1:p.Leu24Pro
NM_001025295.3:c.71T>C MANE Select	NP_001020466.1:p.Leu24Pro