Canonical Allele Identifier: CA2628214313

Gene: PATL2

Linked Data

• gnomAD v4: 15-44711350-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711350T>G , CM000677.2:g.44711350T>G	GRCh38
NC_000015.9:g.45003548T>G , CM000677.1:g.45003548T>G	GRCh37
NC_000015.8:g.42790840T>G	NCBI36
NG_012920.1:g.4864T>G
NG_012920.2:g.4874T>G

Transcript Alleles

HGVS	Amino-acid Change
XM_011521338.1:c.-584A>C	XP_011519640.1:n.-584A>C
XM_011521339.1:c.-465A>C	XP_011519641.1:n.-465A>C
XM_011521340.1:c.-406A>C	XP_011519642.1:n.-406A>C
XM_011521343.1:c.-668A>C	XP_011519645.1:n.-668A>C
XM_011521345.1:c.-639A>C	XP_011519647.1:n.-639A>C
XM_011521338.3:c.-584A>C	XP_011519640.1:n.-584A>C
XM_011521339.3:c.-465A>C	XP_011519641.1:n.-465A>C
XM_011521340.3:c.-406A>C	XP_011519642.1:n.-406A>C
XM_011521343.3:c.-668A>C	XP_011519645.1:n.-668A>C
XM_011521345.3:c.-639A>C	XP_011519647.1:n.-639A>C
NM_001387260.1:c.-94A>C	NP_001374189.1:n.-94A>C