Canonical Allele Identifier: CA396375508

Gene: LCAT

Linked Data

• dbSNP Id: rs2058283795
• MyVariant Identifiers: chr16:g.67973941G>T (hg19) ; chr16:g.67940038G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67940038G>T , CM000678.2:g.67940038G>T	GRCh38
NC_000016.9:g.67973941G>T , CM000678.1:g.67973941G>T	GRCh37
NC_000016.8:g.66531442G>T	NCBI36
NG_009778.1:g.9075C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.1189C>A MANE Select	ENSP00000264005.5:p.His397Asn
ENST00000264005.9:c.1189C>A	ENSP00000264005.5:p.His397Asn
ENST00000570369.5:c.192C>A
ENST00000573538.5:c.927C>A	ENSP00000463220.1:n.927C>A
NM_000229.1:c.1189C>A	NP_000220.1:p.His397Asn
NM_000229.2:c.1189C>A MANE Select	NP_000220.1:p.His397Asn