Canonical Allele Identifier: CA128010792
Gene: PITX1 HGNC NCBI

Linked Data

dbSNP Id: rs762071632
MyVariant Identifiers: chr5:g.134366705C>A (hg19) chr5:g.135031015C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.135031015C>A , CM000667.2:g.135031015C>A GRCh38
NC_000005.9:g.134366705C>A , CM000667.1:g.134366705C>A GRCh37
NC_000005.8:g.134394604C>A NCBI36
NG_012114.1:g.8260G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000265340.12:c.402+261G>T MANE Select ENSP00000265340.6:n.402+261G>T
ENST00000265340.11:c.402+261G>T ENSP00000265340.6:n.402+261G>T
ENST00000503586.1:c.524+261G>T
ENST00000504936.1:n.735+261G>T
ENST00000506438.5:c.402+261G>T ENSP00000427542.1:n.402+261G>T
NM_002653.4:c.402+261G>T NP_002644.4:n.402+261G>T
NM_002653.5:c.402+261G>T MANE Select NP_002644.4:n.402+261G>T
Search 100 bp 5'
Search 100 bp 3'