Canonical Allele Identifier: CA396375720
Gene: LCAT HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.67974046C>G (hg19) chr16:g.67940143C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940143C>G , CM000678.2:g.67940143C>G GRCh38
NC_000016.9:g.67974046C>G , CM000678.1:g.67974046C>G GRCh37
NC_000016.8:g.66531547C>G NCBI36
NG_009778.1:g.8970G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.1084G>C MANE Select ENSP00000264005.5:p.Gly362Arg
ENST00000264005.9:c.1084G>C ENSP00000264005.5:p.Gly362Arg
ENST00000570369.5:c.156-69G>C
ENST00000573538.5:c.822G>C ENSP00000463220.1:n.822G>C
NM_000229.1:c.1084G>C NP_000220.1:p.Gly362Arg
NM_000229.2:c.1084G>C MANE Select NP_000220.1:p.Gly362Arg
Search 100 bp 5'
Search 100 bp 3'