Canonical Allele Identifier: CA496092277
Gene: LCAT HGNC NCBI

Linked Data

dbSNP Id: rs2151319810
gnomAD v3: 16-67939964-G-T
gnomAD v4: 16-67939964-G-T
MyVariant Identifiers: chr16:g.67973867G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67939964G>T , CM000678.2:g.67939964G>T GRCh38
NC_000016.9:g.67973867G>T , CM000678.1:g.67973867G>T GRCh37
NC_000016.8:g.66531368G>T NCBI36
NG_009778.1:g.9149C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.1263C>A MANE Select ENSP00000264005.5:p.Ala421=
ENST00000264005.9:c.1263C>A ENSP00000264005.5:p.Ala421=
ENST00000570369.5:c.266C>A
ENST00000573538.5:c.1001C>A ENSP00000463220.1:n.1001C>A
NM_000229.1:c.1263C>A NP_000220.1:p.Ala421=
NM_000229.2:c.1263C>A MANE Select NP_000220.1:p.Ala421=
Search 100 bp 5'
Search 100 bp 3'