Canonical Allele Identifier: CA2628214321

Gene: B2M PATL2

Linked Data

• gnomAD v4: 15-44711358-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711358A>C , CM000677.2:g.44711358A>C	GRCh38
NC_000015.9:g.45003556A>C , CM000677.1:g.45003556A>C	GRCh37
NC_000015.8:g.42790848A>C	NCBI36
NG_012920.1:g.4872A>C
NG_012920.2:g.4882A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695792.1:n.1A>C (B2M)
XM_011521338.1:c.-592T>G (PATL2)	XP_011519640.1:n.-592T>G
XM_011521339.1:c.-473T>G (PATL2)	XP_011519641.1:n.-473T>G
XM_011521340.1:c.-414T>G (PATL2)	XP_011519642.1:n.-414T>G
XM_011521343.1:c.-676T>G (PATL2)	XP_011519645.1:n.-676T>G
XM_011521345.1:c.-647T>G (PATL2)	XP_011519647.1:n.-647T>G
XM_011521338.3:c.-592T>G (PATL2)	XP_011519640.1:n.-592T>G
XM_011521339.3:c.-473T>G (PATL2)	XP_011519641.1:n.-473T>G
XM_011521340.3:c.-414T>G (PATL2)	XP_011519642.1:n.-414T>G
XM_011521343.3:c.-676T>G (PATL2)	XP_011519645.1:n.-676T>G
XM_011521345.3:c.-647T>G (PATL2)	XP_011519647.1:n.-647T>G
NM_001387260.1:c.-102T>G (PATL2)	NP_001374189.1:n.-102T>G