Canonical Allele Identifier: CA283160392
Gene: LCAT HGNC NCBI

Linked Data

dbSNP Id: rs370588539
gnomAD v4: 16-67940034-C-T
MyVariant Identifiers: chr16:g.67973937C>T (hg19) chr16:g.67940034C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940034C>T , CM000678.2:g.67940034C>T GRCh38
NC_000016.9:g.67973937C>T , CM000678.1:g.67973937C>T GRCh37
NC_000016.8:g.66531438C>T NCBI36
NG_009778.1:g.9079G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.1193G>A MANE Select ENSP00000264005.5:p.Gly398Glu
ENST00000264005.9:c.1193G>A ENSP00000264005.5:p.Gly398Glu
ENST00000570369.5:c.196G>A
ENST00000573538.5:c.931G>A ENSP00000463220.1:n.931G>A
NM_000229.1:c.1193G>A NP_000220.1:p.Gly398Glu
NM_000229.2:c.1193G>A MANE Select NP_000220.1:p.Gly398Glu
Search 100 bp 5'
Search 100 bp 3'