Canonical Allele Identifier: CA396375516
Gene: LCAT HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.67973946G>T (hg19) chr16:g.67940043G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940043G>T , CM000678.2:g.67940043G>T GRCh38
NC_000016.9:g.67973946G>T , CM000678.1:g.67973946G>T GRCh37
NC_000016.8:g.66531447G>T NCBI36
NG_009778.1:g.9070C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.1184C>A MANE Select ENSP00000264005.5:p.Pro395His
ENST00000264005.9:c.1184C>A ENSP00000264005.5:p.Pro395His
ENST00000570369.5:c.187C>A
ENST00000573538.5:c.922C>A ENSP00000463220.1:n.922C>A
NM_000229.1:c.1184C>A NP_000220.1:p.Pro395His
NM_000229.2:c.1184C>A MANE Select NP_000220.1:p.Pro395His
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