Canonical Allele Identifier: CA496384119
Gene: LCAT HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.67974188G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940285G>C , CM000678.2:g.67940285G>C GRCh38
NC_000016.9:g.67974188G>C , CM000678.1:g.67974188G>C GRCh37
NC_000016.8:g.66531689G>C NCBI36
NG_009778.1:g.8828C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264005.10:c.942C>G MANE Select ENSP00000264005.5:p.Gly314=
ENST00000264005.9:c.942C>G ENSP00000264005.5:p.Gly314=
ENST00000570369.5:c.156-211C>G
ENST00000570980.1:c.726C>G ENSP00000464651.1:p.Gly242=
ENST00000573538.5:c.680C>G ENSP00000463220.1:n.680C>G
NM_000229.1:c.942C>G NP_000220.1:p.Gly314=
NM_000229.2:c.942C>G MANE Select NP_000220.1:p.Gly314=
Search 100 bp 5'
Search 100 bp 3'