Canonical Allele Identifier: CA2633852008
Gene: LCAT HGNC NCBI

Linked Data

gnomAD v4: 16-67940827-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940827T>C , CM000678.2:g.67940827T>C GRCh38
NC_000016.9:g.67974730T>C , CM000678.1:g.67974730T>C GRCh37
NC_000016.8:g.66532231T>C NCBI36
NG_009778.1:g.8286A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.749-349A>G MANE Select ENSP00000264005.5:n.749-349A>G
ENST00000264005.9:c.749-349A>G ENSP00000264005.5:n.749-349A>G
ENST00000570369.5:c.156-753A>G
ENST00000570980.1:c.533-349A>G ENSP00000464651.1:n.533-349A>G
ENST00000573538.5:c.396A>G ENSP00000463220.1:p.Thr132=
NM_000229.1:c.749-349A>G NP_000220.1:n.749-349A>G
NM_000229.2:c.749-349A>G MANE Select NP_000220.1:n.749-349A>G
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