Canonical Allele Identifier: CA1540331969
Gene: LIFR HGNC NCBI
LIFR-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs2071237

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.38595604C>A , CM000667.2:g.38595604C>A GRCh38
NC_000005.9:g.38595706C>A , CM000667.1:g.38595706C>A GRCh37
NC_000005.8:g.38631463C>A NCBI36
NG_011817.1:g.4802G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000507786.1:n.306-221G>T (LIFR)
NR_103553.1:n.2540+535C>A (LIFR-AS1)
NR_103554.1:n.2540+535C>A (LIFR-AS1)
XM_017009463.1:c.-142-221G>T (LIFR) XP_016864952.1:n.-142-221G>T