Canonical Allele Identifier: CA3242499

Gene: LIFR

Linked Data

• ClinVar Variation Id: 797713
• ClinVar RCV Id: RCV000981187 ; RCV001271677
• dbSNP Id: rs745548189
• ExAC: 5:38481859 A / G
• gnomAD v2: 5-38481859-A-G
• gnomAD v3: 5-38481757-A-G
• gnomAD v4: 5-38481757-A-G
• MyVariant Identifiers: chr5:g.38481859A>G (hg19) ; chr5:g.38481757A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.38481757A>G , CM000667.2:g.38481757A>G	GRCh38
NC_000005.9:g.38481859A>G , CM000667.1:g.38481859A>G	GRCh37
NC_000005.8:g.38517616A>G	NCBI36
NG_011817.1:g.118649T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453190.7:c.3132T>C MANE Select	ENSP00000398368.2:p.Ser1044=
ENST00000263409.8:c.3132T>C	ENSP00000263409.4:p.Ser1044=
ENST00000453190.6:c.3132T>C	ENSP00000398368.2:p.Ser1044=
NM_001127671.1:c.3132T>C	NP_001121143.1:p.Ser1044=
NM_002310.5:c.3132T>C	NP_002301.1:p.Ser1044=
XM_011514040.1:c.3132T>C	XP_011512342.1:p.Ser1044=
XM_011514041.1:c.3132T>C	XP_011512343.1:p.Ser1044=
XM_011514042.1:c.3132T>C	XP_011512344.1:p.Ser1044=
NM_001364297.1:c.3132T>C	NP_001351226.1:p.Ser1044=
NM_001364298.1:c.3099T>C	NP_001351227.1:p.Ser1033=
XM_011514042.3:c.3132T>C	XP_011512344.1:p.Ser1044=
XM_017009462.1:c.3186T>C	XP_016864951.1:p.Ser1062=
XM_017009463.1:c.3132T>C	XP_016864952.1:p.Ser1044=
NM_001127671.2:c.3132T>C MANE Select	NP_001121143.1:p.Ser1044=
NM_002310.6:c.3132T>C	NP_002301.1:p.Ser1044=
NM_001364297.2:c.3132T>C	NP_001351226.1:p.Ser1044=
NM_001364298.2:c.3099T>C	NP_001351227.1:p.Ser1033=