Canonical Allele Identifier: CA396376452
Gene: LCAT HGNC NCBI

Linked Data

dbSNP Id: rs2151320023

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940480T>C , CM000678.2:g.67940480T>C GRCh38
NC_000016.9:g.67974383T>C , CM000678.1:g.67974383T>C GRCh37
NC_000016.8:g.66531884T>C NCBI36
NG_009778.1:g.8633A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264005.10:c.749-2A>G MANE Select ENSP00000264005.5:n.749-2A>G
ENST00000264005.9:c.749-2A>G ENSP00000264005.5:n.749-2A>G
ENST00000570369.5:c.156-406A>G
ENST00000570980.1:c.533-2A>G ENSP00000464651.1:n.533-2A>G
ENST00000573538.5:c.487-2A>G ENSP00000463220.1:n.487-2A>G
NM_000229.1:c.749-2A>G NP_000220.1:n.749-2A>G
NM_000229.2:c.749-2A>G MANE Select NP_000220.1:n.749-2A>G