Canonical Allele Identifier: CA2173753269

Gene: B2M PATL2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711388A= , CM000677.2:g.44711388A=	GRCh38
NC_000015.9:g.45003586A= , CM000677.1:g.45003586A=	GRCh37
NC_000015.8:g.42790878A=	NCBI36
NG_012920.1:g.4902A=
NG_012920.2:g.4912A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695792.1:n.31A= (B2M)
XM_011521338.1:c.-622T= (PATL2)	XP_011519640.1:n.-622T=
XM_011521339.1:c.-503T= (PATL2)	XP_011519641.1:n.-503T=
XM_011521340.1:c.-444T= (PATL2)	XP_011519642.1:n.-444T=
XM_011521343.1:c.-706T= (PATL2)	XP_011519645.1:n.-706T=
XM_011521345.1:c.-677T= (PATL2)	XP_011519647.1:n.-677T=
XM_011521338.3:c.-622T= (PATL2)	XP_011519640.1:n.-622T=
XM_011521339.3:c.-503T= (PATL2)	XP_011519641.1:n.-503T=
XM_011521340.3:c.-444T= (PATL2)	XP_011519642.1:n.-444T=
XM_011521343.3:c.-706T= (PATL2)	XP_011519645.1:n.-706T=
XM_011521345.3:c.-677T= (PATL2)	XP_011519647.1:n.-677T=
NM_001387260.1:c.-132T= (PATL2)	NP_001374189.1:n.-132T=