Canonical Allele Identifier: CA752803697

Gene:

Linked Data

• dbSNP Id: rs1344388400
• gnomAD v3: 22-36129893-G-A
• gnomAD v4: 22-36129893-G-A
• MyVariant Identifiers: chr22:g.36525941G>A (hg19) ; chr22:g.36129893G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36129893G>A , CM000684.2:g.36129893G>A	GRCh38
NC_000022.10:g.36525941G>A , CM000684.1:g.36525941G>A	GRCh37
NC_000022.9:g.34855887G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_430441.2:n.1547+3269C>T
XR_938219.1:n.3043C>T
XR_938220.1:n.3043C>T
XR_938221.1:n.1471+3969C>T
XR_001755516.2:n.4905C>T
XR_001755517.2:n.3132C>T
XR_001755518.2:n.4905C>T
XR_001755519.2:n.4905C>T
XR_001755520.2:n.4905C>T
XR_001755521.2:n.4905C>T
XR_001755522.2:n.1637-2120C>T
XR_001755525.2:n.1637-539C>T
XR_001755526.2:n.1637-2120C>T
XR_430441.4:n.1636+3269C>T