Canonical Allele Identifier: CA885547875

Gene: RAP1A

Linked Data

• dbSNP Id: rs1331193780
• gnomAD v3: 1-111565079-G-A
• gnomAD v4: 1-111565079-G-A
• MyVariant Identifiers: chr1:g.112107701G>A (hg19) ; chr1:g.111565079G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.111565079G>A , CM000663.2:g.111565079G>A	GRCh38
NC_000001.10:g.112107701G>A , CM000663.1:g.112107701G>A	GRCh37
NC_000001.9:g.111909224G>A	NCBI36
NG_032119.1:g.3897C>T , LRG_424:g.3897C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356415.5:c.-28+22570G>A	ENSP00000348786.1:n.-28+22570G>A
XM_017001964.1:c.-28+22570G>A	XP_016857453.1:n.-28+22570G>A
NM_001370216.1:c.-28+22570G>A	NP_001357145.1:n.-28+22570G>A
NM_001370216.2:c.-28+22570G>A	NP_001357145.1:n.-28+22570G>A