Canonical Allele Identifier: CA2633851129
Gene: LCAT HGNC NCBI

Linked Data

gnomAD v4: 16-67940495-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940495A>T , CM000678.2:g.67940495A>T GRCh38
NC_000016.9:g.67974398A>T , CM000678.1:g.67974398A>T GRCh37
NC_000016.8:g.66531899A>T NCBI36
NG_009778.1:g.8618T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.749-17T>A MANE Select ENSP00000264005.5:n.749-17T>A
ENST00000264005.9:c.749-17T>A ENSP00000264005.5:n.749-17T>A
ENST00000570369.5:c.156-421T>A
ENST00000570980.1:c.533-17T>A ENSP00000464651.1:n.533-17T>A
ENST00000573538.5:c.487-17T>A ENSP00000463220.1:n.487-17T>A
NM_000229.1:c.749-17T>A NP_000220.1:n.749-17T>A
NM_000229.2:c.749-17T>A MANE Select NP_000220.1:n.749-17T>A
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