Canonical Allele Identifier: CA396375392
Gene: LCAT HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.67973890T>G (hg19) chr16:g.67939987T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67939987T>G , CM000678.2:g.67939987T>G GRCh38
NC_000016.9:g.67973890T>G , CM000678.1:g.67973890T>G GRCh37
NC_000016.8:g.66531391T>G NCBI36
NG_009778.1:g.9126A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.1240A>C MANE Select ENSP00000264005.5:p.Ile414Leu
ENST00000264005.9:c.1240A>C ENSP00000264005.5:p.Ile414Leu
ENST00000570369.5:c.243A>C
ENST00000573538.5:c.978A>C ENSP00000463220.1:n.978A>C
NM_000229.1:c.1240A>C NP_000220.1:p.Ile414Leu
NM_000229.2:c.1240A>C MANE Select NP_000220.1:p.Ile414Leu
Search 100 bp 5'
Search 100 bp 3'