Canonical Allele Identifier: CA496383980
Gene: LCAT HGNC NCBI

Linked Data

dbSNP Id: rs959668537
gnomAD v2: 16-67974260-A-G
gnomAD v4: 16-67940357-A-G
MyVariant Identifiers: chr16:g.67974260A>G (hg19) chr16:g.67940357A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940357A>G , CM000678.2:g.67940357A>G GRCh38
NC_000016.9:g.67974260A>G , CM000678.1:g.67974260A>G GRCh37
NC_000016.8:g.66531761A>G NCBI36
NG_009778.1:g.8756T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.870T>C MANE Select ENSP00000264005.5:p.Ile290=
ENST00000264005.9:c.870T>C ENSP00000264005.5:p.Ile290=
ENST00000570369.5:c.156-283T>C
ENST00000570980.1:c.654T>C ENSP00000464651.1:p.Ile218=
ENST00000573538.5:c.608T>C ENSP00000463220.1:n.608T>C
NM_000229.1:c.870T>C NP_000220.1:p.Ile290=
NM_000229.2:c.870T>C MANE Select NP_000220.1:p.Ile290=
Search 100 bp 5'
Search 100 bp 3'