Canonical Allele Identifier: CA622937054
Gene: LCAT HGNC NCBI

Linked Data

dbSNP Id: rs1404391135
gnomAD v2: 16-67974736-T-A
gnomAD v3: 16-67940833-T-A
gnomAD v4: 16-67940833-T-A
MyVariant Identifiers: chr16:g.67974736T>A (hg19) chr16:g.67974736_67974738delinsAAC (hg19) chr16:g.67940833T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940833T>A , CM000678.2:g.67940833T>A GRCh38
NC_000016.9:g.67974736T>A , CM000678.1:g.67974736T>A GRCh37
NC_000016.8:g.66532237T>A NCBI36
NG_009778.1:g.8280A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.749-355A>T MANE Select ENSP00000264005.5:n.749-355A>T
ENST00000264005.9:c.749-355A>T ENSP00000264005.5:n.749-355A>T
ENST00000570369.5:c.156-759A>T
ENST00000570980.1:c.533-355A>T ENSP00000464651.1:n.533-355A>T
ENST00000573538.5:c.392-2A>T ENSP00000463220.1:n.392-2A>T
NM_000229.1:c.749-355A>T NP_000220.1:n.749-355A>T
NM_000229.2:c.749-355A>T MANE Select NP_000220.1:n.749-355A>T
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