Canonical Allele Identifier: CA283161292
Gene: LCAT HGNC NCBI

Linked Data

dbSNP Id: rs993461594
MyVariant Identifiers: chr16:g.67940707A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940707A>C , CM000678.2:g.67940707A>C GRCh38
NC_000016.9:g.67974610A>C , CM000678.1:g.67974610A>C GRCh37
NC_000016.8:g.66532111A>C NCBI36
NG_009778.1:g.8406T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.749-229T>G MANE Select ENSP00000264005.5:n.749-229T>G
ENST00000264005.9:c.749-229T>G ENSP00000264005.5:n.749-229T>G
ENST00000570369.5:c.156-633T>G
ENST00000570980.1:c.533-229T>G ENSP00000464651.1:n.533-229T>G
ENST00000573538.5:c.486+30T>G ENSP00000463220.1:n.486+30T>G
NM_000229.1:c.749-229T>G NP_000220.1:n.749-229T>G
NM_000229.2:c.749-229T>G MANE Select NP_000220.1:n.749-229T>G
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