Canonical Allele Identifier: CA496384121
Gene: LCAT HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.67974191T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940288T>C , CM000678.2:g.67940288T>C GRCh38
NC_000016.9:g.67974191T>C , CM000678.1:g.67974191T>C GRCh37
NC_000016.8:g.66531692T>C NCBI36
NG_009778.1:g.8825A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.939A>G MANE Select ENSP00000264005.5:p.Glu313=
ENST00000264005.9:c.939A>G ENSP00000264005.5:p.Glu313=
ENST00000570369.5:c.156-214A>G
ENST00000570980.1:c.723A>G ENSP00000464651.1:p.Glu241=
ENST00000573538.5:c.677A>G ENSP00000463220.1:n.677A>G
NM_000229.1:c.939A>G NP_000220.1:p.Glu313=
NM_000229.2:c.939A>G MANE Select NP_000220.1:p.Glu313=