Canonical Allele Identifier: CA8120969
Gene: LCAT HGNC NCBI

Linked Data

dbSNP Id: rs183693878
ExAC: 16:67974666 C / T
gnomAD v2: 16-67974666-C-T
gnomAD v3: 16-67940763-C-T
gnomAD v4: 16-67940763-C-T
MyVariant Identifiers: chr16:g.67974666C>T (hg19) chr16:g.67940763C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940763C>T , CM000678.2:g.67940763C>T GRCh38
NC_000016.9:g.67974666C>T , CM000678.1:g.67974666C>T GRCh37
NC_000016.8:g.66532167C>T NCBI36
NG_009778.1:g.8350G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.749-285G>A MANE Select ENSP00000264005.5:n.749-285G>A
ENST00000264005.9:c.749-285G>A ENSP00000264005.5:n.749-285G>A
ENST00000570369.5:c.156-689G>A
ENST00000570980.1:c.533-285G>A ENSP00000464651.1:n.533-285G>A
ENST00000573538.5:c.460G>A ENSP00000463220.1:n.460G>A
NM_000229.1:c.749-285G>A NP_000220.1:n.749-285G>A
NM_000229.2:c.749-285G>A MANE Select NP_000220.1:n.749-285G>A
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