Canonical Allele Identifier: CA2628214306

Gene: PATL2

Linked Data

• gnomAD v4: 15-44711336-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711336T>C , CM000677.2:g.44711336T>C	GRCh38
NC_000015.9:g.45003534T>C , CM000677.1:g.45003534T>C	GRCh37
NC_000015.8:g.42790826T>C	NCBI36
NG_012920.1:g.4850T>C
NG_012920.2:g.4860T>C

Transcript Alleles

HGVS	Amino-acid Change
XM_011521338.1:c.-570A>G	XP_011519640.1:n.-570A>G
XM_011521339.1:c.-451A>G	XP_011519641.1:n.-451A>G
XM_011521340.1:c.-392A>G	XP_011519642.1:n.-392A>G
XM_011521343.1:c.-654A>G	XP_011519645.1:n.-654A>G
XM_011521345.1:c.-625A>G	XP_011519647.1:n.-625A>G
XM_011521338.3:c.-570A>G	XP_011519640.1:n.-570A>G
XM_011521339.3:c.-451A>G	XP_011519641.1:n.-451A>G
XM_011521340.3:c.-392A>G	XP_011519642.1:n.-392A>G
XM_011521343.3:c.-654A>G	XP_011519645.1:n.-654A>G
XM_011521345.3:c.-625A>G	XP_011519647.1:n.-625A>G
NM_001387260.1:c.-80A>G	NP_001374189.1:n.-80A>G