Canonical Allele Identifier: CA2577107637

Gene: LCT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135789556A>G , CM000664.2:g.135789556A>G	GRCh38
NC_000002.11:g.136547126A>G , CM000664.1:g.136547126A>G	GRCh37
NC_000002.10:g.136263596A>G	NCBI36
NG_008104.2:g.70614T>C , LRG_338:g.70614T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000264162.7:c.5563+15T>C MANE Select	ENSP00000264162.2:n.5563+15T>C
ENST00000264162.6:c.5563+15T>C	ENSP00000264162.2:n.5563+15T>C
NM_002299.2:c.5563+15T>C , LRG_338t1:c.5563+15T>C	NP_002290.2:n.5563+15T>C
NM_002299.3:c.5563+15T>C	NP_002290.2:n.5563+15T>C
NM_002299.4:c.5563+15T>C MANE Select	NP_002290.2:n.5563+15T>C