Canonical Allele Identifier: CA283161220
Gene: LCAT HGNC NCBI

Linked Data

dbSNP Id: rs943928664
gnomAD v2: 16-67974538-A-T
gnomAD v3: 16-67940635-A-T
gnomAD v4: 16-67940635-A-T
MyVariant Identifiers: chr16:g.67974538A>T (hg19) chr16:g.67940635A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940635A>T , CM000678.2:g.67940635A>T GRCh38
NC_000016.9:g.67974538A>T , CM000678.1:g.67974538A>T GRCh37
NC_000016.8:g.66532039A>T NCBI36
NG_009778.1:g.8478T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.749-157T>A MANE Select ENSP00000264005.5:n.749-157T>A
ENST00000264005.9:c.749-157T>A ENSP00000264005.5:n.749-157T>A
ENST00000570369.5:c.156-561T>A
ENST00000570980.1:c.533-157T>A ENSP00000464651.1:n.533-157T>A
ENST00000573538.5:c.486+102T>A ENSP00000463220.1:n.486+102T>A
NM_000229.1:c.749-157T>A NP_000220.1:n.749-157T>A
NM_000229.2:c.749-157T>A MANE Select NP_000220.1:n.749-157T>A
Search 100 bp 5'
Search 100 bp 3'