Canonical Allele Identifier: CA713086330

Gene: PATL2

Linked Data

• dbSNP Id: rs1260962398
• gnomAD v3: 15-44711347-C-T
• gnomAD v4: 15-44711347-C-T
• MyVariant Identifiers: chr15:g.45003545C>T (hg19) ; chr15:g.44711347C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711347C>T , CM000677.2:g.44711347C>T	GRCh38
NC_000015.9:g.45003545C>T , CM000677.1:g.45003545C>T	GRCh37
NC_000015.8:g.42790837C>T	NCBI36
NG_012920.1:g.4861C>T
NG_012920.2:g.4871C>T

Transcript Alleles

HGVS	Amino-acid Change
XM_011521338.1:c.-581G>A	XP_011519640.1:n.-581G>A
XM_011521339.1:c.-462G>A	XP_011519641.1:n.-462G>A
XM_011521340.1:c.-403G>A	XP_011519642.1:n.-403G>A
XM_011521343.1:c.-665G>A	XP_011519645.1:n.-665G>A
XM_011521345.1:c.-636G>A	XP_011519647.1:n.-636G>A
XM_011521338.3:c.-581G>A	XP_011519640.1:n.-581G>A
XM_011521339.3:c.-462G>A	XP_011519641.1:n.-462G>A
XM_011521340.3:c.-403G>A	XP_011519642.1:n.-403G>A
XM_011521343.3:c.-665G>A	XP_011519645.1:n.-665G>A
XM_011521345.3:c.-636G>A	XP_011519647.1:n.-636G>A
NM_001387260.1:c.-91G>A	NP_001374189.1:n.-91G>A