Canonical Allele Identifier: CA396375358
Gene: LCAT HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.67973874A>T (hg19) chr16:g.67939971A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67939971A>T , CM000678.2:g.67939971A>T GRCh38
NC_000016.9:g.67973874A>T , CM000678.1:g.67973874A>T GRCh37
NC_000016.8:g.66531375A>T NCBI36
NG_009778.1:g.9142T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.1256T>A MANE Select ENSP00000264005.5:p.Leu419Gln
ENST00000264005.9:c.1256T>A ENSP00000264005.5:p.Leu419Gln
ENST00000570369.5:c.259T>A
ENST00000573538.5:c.994T>A ENSP00000463220.1:n.994T>A
NM_000229.1:c.1256T>A NP_000220.1:p.Leu419Gln
NM_000229.2:c.1256T>A MANE Select NP_000220.1:p.Leu419Gln
Search 100 bp 5'
Search 100 bp 3'