Canonical Allele Identifier: CA2597452035
Gene: LCAT HGNC NCBI

Linked Data

dbSNP Id: rs2058287623
gnomAD v3: 16-67940836-A-G
gnomAD v4: 16-67940836-A-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940836A>G , CM000678.2:g.67940836A>G GRCh38
NC_000016.9:g.67974739A>G , CM000678.1:g.67974739A>G GRCh37
NC_000016.8:g.66532240A>G NCBI36
NG_009778.1:g.8277T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.749-358T>C MANE Select ENSP00000264005.5:n.749-358T>C
ENST00000264005.9:c.749-358T>C ENSP00000264005.5:n.749-358T>C
ENST00000570369.5:c.156-762T>C
ENST00000570980.1:c.533-358T>C ENSP00000464651.1:n.533-358T>C
ENST00000573538.5:c.392-5T>C ENSP00000463220.1:n.392-5T>C
NM_000229.1:c.749-358T>C NP_000220.1:n.749-358T>C
NM_000229.2:c.749-358T>C MANE Select NP_000220.1:n.749-358T>C
Search 100 bp 5'
Search 100 bp 3'