Canonical Allele Identifier: CA10178342

Gene: LIF

Linked Data

• ClinVar Variation Id: 403032
• ClinVar RCV Id: RCV000455358 ; RCV003424004
• dbSNP Id: rs41281637
• ExAC: 22:30639993 C / T
• gnomAD v2: 22-30639993-C-T
• gnomAD v3: 22-30244004-C-T
• gnomAD v4: 22-30244004-C-T
• MyVariant Identifiers: chr22:g.30639993C>T (hg19) ; chr22:g.30244004C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30244004C>T , CM000684.2:g.30244004C>T	GRCh38
NC_000022.10:g.30639993C>T , CM000684.1:g.30639993C>T	GRCh37
NC_000022.9:g.28969993C>T	NCBI36
NG_008721.1:g.7804G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249075.4:c.256G>A MANE Select	ENSP00000249075.3:p.Val86Met
ENST00000249075.3:c.256G>A	ENSP00000249075.3:p.Val86Met
ENST00000403987.3:c.77G>A	ENSP00000384450.3:p.Arg26His
NM_001257135.1:c.77G>A	NP_001244064.1:p.Arg26His
NM_002309.4:c.256G>A	NP_002300.1:p.Val86Met
XM_006724240.2:c.256G>A	XP_006724303.1:p.Val86Met
XM_011530172.1:c.256G>A	XP_011528474.1:p.Val86Met
XM_024452239.1:c.256G>A	XP_024308007.1:p.Val86Met
XM_024452240.1:c.256G>A	XP_024308008.1:p.Val86Met
NM_002309.5:c.256G>A MANE Select	NP_002300.1:p.Val86Met
NM_001257135.2:c.77G>A	NP_001244064.1:p.Arg26His