Canonical Allele Identifier: CA396376095
Gene: LCAT HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.67974223G>C (hg19) chr16:g.67940320G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940320G>C , CM000678.2:g.67940320G>C GRCh38
NC_000016.9:g.67974223G>C , CM000678.1:g.67974223G>C GRCh37
NC_000016.8:g.66531724G>C NCBI36
NG_009778.1:g.8793C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.907C>G MANE Select ENSP00000264005.5:p.Gln303Glu
ENST00000264005.9:c.907C>G ENSP00000264005.5:p.Gln303Glu
ENST00000570369.5:c.156-246C>G
ENST00000570980.1:c.691C>G ENSP00000464651.1:p.Gln231Glu
ENST00000573538.5:c.645C>G ENSP00000463220.1:n.645C>G
NM_000229.1:c.907C>G NP_000220.1:p.Gln303Glu
NM_000229.2:c.907C>G MANE Select NP_000220.1:p.Gln303Glu
Search 100 bp 5'
Search 100 bp 3'