Canonical Allele Identifier: CA2628214341

Gene: B2M PATL2

Linked Data

• gnomAD v4: 15-44711372-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711372A>G , CM000677.2:g.44711372A>G	GRCh38
NC_000015.9:g.45003570A>G , CM000677.1:g.45003570A>G	GRCh37
NC_000015.8:g.42790862A>G	NCBI36
NG_012920.1:g.4886A>G
NG_012920.2:g.4896A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695792.1:n.15A>G (B2M)
XM_011521338.1:c.-606T>C (PATL2)	XP_011519640.1:n.-606T>C
XM_011521339.1:c.-487T>C (PATL2)	XP_011519641.1:n.-487T>C
XM_011521340.1:c.-428T>C (PATL2)	XP_011519642.1:n.-428T>C
XM_011521343.1:c.-690T>C (PATL2)	XP_011519645.1:n.-690T>C
XM_011521345.1:c.-661T>C (PATL2)	XP_011519647.1:n.-661T>C
XM_011521338.3:c.-606T>C (PATL2)	XP_011519640.1:n.-606T>C
XM_011521339.3:c.-487T>C (PATL2)	XP_011519641.1:n.-487T>C
XM_011521340.3:c.-428T>C (PATL2)	XP_011519642.1:n.-428T>C
XM_011521343.3:c.-690T>C (PATL2)	XP_011519645.1:n.-690T>C
XM_011521345.3:c.-661T>C (PATL2)	XP_011519647.1:n.-661T>C
NM_001387260.1:c.-116T>C (PATL2)	NP_001374189.1:n.-116T>C