Canonical Allele Identifier: CA2633848201
Gene: LCAT HGNC NCBI

Linked Data

gnomAD v4: 16-67942984-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67942984G>T , CM000678.2:g.67942984G>T GRCh38
NC_000016.9:g.67976887G>T , CM000678.1:g.67976887G>T GRCh37
NC_000016.8:g.66534388G>T NCBI36
NG_009778.1:g.6129C>A
NG_033098.1:g.30711C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264005.10:c.312-8C>A MANE Select ENSP00000264005.5:n.312-8C>A
ENST00000264005.9:c.312-8C>A ENSP00000264005.5:n.312-8C>A
ENST00000570369.5:c.40-8C>A
ENST00000570980.1:c.96-8C>A ENSP00000464651.1:n.96-8C>A
ENST00000575277.1:n.90-8C>A
ENST00000575467.5:c.*7-8C>A ENSP00000460653.1:n.*7-8C>A
NM_000229.1:c.312-8C>A NP_000220.1:n.312-8C>A
NM_000229.2:c.312-8C>A MANE Select NP_000220.1:n.312-8C>A
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