Canonical Allele Identifier: CA396376338
Gene: LCAT HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.67974334C>G (hg19) chr16:g.67940431C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940431C>G , CM000678.2:g.67940431C>G GRCh38
NC_000016.9:g.67974334C>G , CM000678.1:g.67974334C>G GRCh37
NC_000016.8:g.66531835C>G NCBI36
NG_009778.1:g.8682G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.796G>C MANE Select ENSP00000264005.5:p.Glu266Gln
ENST00000264005.9:c.796G>C ENSP00000264005.5:p.Glu266Gln
ENST00000570369.5:c.156-357G>C
ENST00000570980.1:c.580G>C ENSP00000464651.1:p.Glu194Gln
ENST00000573538.5:c.534G>C ENSP00000463220.1:n.534G>C
NM_000229.1:c.796G>C NP_000220.1:p.Glu266Gln
NM_000229.2:c.796G>C MANE Select NP_000220.1:p.Glu266Gln
Search 100 bp 5'
Search 100 bp 3'