Canonical Allele Identifier: CA2628214343

Gene: B2M PATL2

Linked Data

• gnomAD v4: 15-44711372-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711373dup , CM000677.2:g.44711373dup	GRCh38
NC_000015.9:g.45003571dup , CM000677.1:g.45003571dup	GRCh37
NC_000015.8:g.42790863dup	NCBI36
NG_012920.1:g.4887dup
NG_012920.2:g.4897dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695792.1:n.16dup (B2M)
XM_011521338.1:c.-607dup (PATL2)	XP_011519640.1:n.-607dup
XM_011521339.1:c.-488dup (PATL2)	XP_011519641.1:n.-488dup
XM_011521340.1:c.-429dup (PATL2)	XP_011519642.1:n.-429dup
XM_011521343.1:c.-691dup (PATL2)	XP_011519645.1:n.-691dup
XM_011521345.1:c.-662dup (PATL2)	XP_011519647.1:n.-662dup
XM_011521338.3:c.-607dup (PATL2)	XP_011519640.1:n.-607dup
XM_011521339.3:c.-488dup (PATL2)	XP_011519641.1:n.-488dup
XM_011521340.3:c.-429dup (PATL2)	XP_011519642.1:n.-429dup
XM_011521343.3:c.-691dup (PATL2)	XP_011519645.1:n.-691dup
XM_011521345.3:c.-662dup (PATL2)	XP_011519647.1:n.-662dup
NM_001387260.1:c.-117dup (PATL2)	NP_001374189.1:n.-117dup