Canonical Allele Identifier: CA396376126
Gene: LCAT HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.67974239G>C (hg19) chr16:g.67940336G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940336G>C , CM000678.2:g.67940336G>C GRCh38
NC_000016.9:g.67974239G>C , CM000678.1:g.67974239G>C GRCh37
NC_000016.8:g.66531740G>C NCBI36
NG_009778.1:g.8777C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.891C>G MANE Select ENSP00000264005.5:p.Tyr297Ter
ENST00000264005.9:c.891C>G ENSP00000264005.5:p.Tyr297Ter
ENST00000570369.5:c.156-262C>G
ENST00000570980.1:c.675C>G ENSP00000464651.1:p.Tyr225Ter
ENST00000573538.5:c.629C>G ENSP00000463220.1:n.629C>G
NM_000229.1:c.891C>G NP_000220.1:p.Tyr297Ter
NM_000229.2:c.891C>G MANE Select NP_000220.1:p.Tyr297Ter
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