Canonical Allele Identifier: CA496383888

Gene: LCAT

Linked Data

• dbSNP Id: rs2058284442
• MyVariant Identifiers: chr16:g.67974035A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67940132A>G , CM000678.2:g.67940132A>G	GRCh38
NC_000016.9:g.67974035A>G , CM000678.1:g.67974035A>G	GRCh37
NC_000016.8:g.66531536A>G	NCBI36
NG_009778.1:g.8981T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.1095T>C MANE Select	ENSP00000264005.5:p.Tyr365=
ENST00000264005.9:c.1095T>C	ENSP00000264005.5:p.Tyr365=
ENST00000570369.5:c.156-58T>C
ENST00000573538.5:c.833T>C	ENSP00000463220.1:n.833T>C
NM_000229.1:c.1095T>C	NP_000220.1:p.Tyr365=
NM_000229.2:c.1095T>C MANE Select	NP_000220.1:p.Tyr365=