Canonical Allele Identifier: CA8120950
Gene: LCAT HGNC NCBI

Linked Data

dbSNP Id: rs751222702
ExAC: 16:67974302 C / T
gnomAD v2: 16-67974302-C-T
gnomAD v4: 16-67940399-C-T
MyVariant Identifiers: chr16:g.67974302C>T (hg19) chr16:g.67940399C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940399C>T , CM000678.2:g.67940399C>T GRCh38
NC_000016.9:g.67974302C>T , CM000678.1:g.67974302C>T GRCh37
NC_000016.8:g.66531803C>T NCBI36
NG_009778.1:g.8714G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.828G>A MANE Select ENSP00000264005.5:p.Met276Ile
ENST00000264005.9:c.828G>A ENSP00000264005.5:p.Met276Ile
ENST00000570369.5:c.156-325G>A
ENST00000570980.1:c.612G>A ENSP00000464651.1:p.Met204Ile
ENST00000573538.5:c.566G>A ENSP00000463220.1:n.566G>A
NM_000229.1:c.828G>A NP_000220.1:p.Met276Ile
NM_000229.2:c.828G>A MANE Select NP_000220.1:p.Met276Ile
Search 100 bp 5'
Search 100 bp 3'