Canonical Allele Identifier: CA718049785

Gene: LITAF

Linked Data

• dbSNP Id: rs1277535691
• MyVariant Identifiers: chr16:g.11691679A>G (hg19) ; chr16:g.11597823A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.11597823A>G , CM000678.2:g.11597823A>G	GRCh38
NC_000016.9:g.11691679A>G , CM000678.1:g.11691679A>G	GRCh37
NC_000016.8:g.11599180A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000571627.5:c.-6+565T>C	ENSP00000460743.1:n.-6+565T>C
ENST00000574848.5:c.85+35710T>C	ENSP00000459898.1:n.85+35710T>C
ENST00000576036.5:c.-6+31300T>C	ENSP00000461667.1:n.-6+31300T>C
ENST00000576334.1:c.85+35710T>C	ENSP00000458538.1:n.85+35710T>C
XM_011522754.1:c.85+35710T>C	XP_011521056.1:n.85+35710T>C
XM_011522754.3:c.85+35710T>C	XP_011521056.1:n.85+35710T>C
XM_017023896.1:c.-6+31300T>C	XP_016879385.1:n.-6+31300T>C