Canonical Allele Identifier: CA496384123
Gene: LCAT HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.67974200G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940297G>A , CM000678.2:g.67940297G>A GRCh38
NC_000016.9:g.67974200G>A , CM000678.1:g.67974200G>A GRCh37
NC_000016.8:g.66531701G>A NCBI36
NG_009778.1:g.8816C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.930C>T MANE Select ENSP00000264005.5:p.His310=
ENST00000264005.9:c.930C>T ENSP00000264005.5:p.His310=
ENST00000570369.5:c.156-223C>T
ENST00000570980.1:c.714C>T ENSP00000464651.1:p.His238=
ENST00000573538.5:c.668C>T ENSP00000463220.1:n.668C>T
NM_000229.1:c.930C>T NP_000220.1:p.His310=
NM_000229.2:c.930C>T MANE Select NP_000220.1:p.His310=