Canonical Allele Identifier: CA1008679016

Gene: LMX1A

Linked Data

• dbSNP Id: rs1655315906
• gnomAD v3: 1-165319368-T-C
• gnomAD v4: 1-165319368-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165319368T>C , CM000663.2:g.165319368T>C	GRCh38
NC_000001.10:g.165288605T>C , CM000663.1:g.165288605T>C	GRCh37
NC_000001.9:g.163555229T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294816.6:c.263+33708A>G	ENSP00000294816.2:n.263+33708A>G
ENST00000342310.7:c.263+33708A>G MANE Select	ENSP00000340226.3:n.263+33708A>G
ENST00000367893.4:c.263+33708A>G	ENSP00000356868.4:n.263+33708A>G
NM_001174069.1:c.263+33708A>G	NP_001167540.1:n.263+33708A>G
NM_177398.3:c.263+33708A>G	NP_796372.1:n.263+33708A>G
XM_011509540.1:c.263+33708A>G	XP_011507842.1:n.263+33708A>G
XM_011509540.2:c.263+33708A>G	XP_011507842.1:n.263+33708A>G
NM_177398.4:c.263+33708A>G MANE Select	NP_796372.1:n.263+33708A>G
NM_001174069.2:c.263+33708A>G	NP_001167540.1:n.263+33708A>G