Canonical Allele Identifier: CA824297173

Gene: CDKN1A

Linked Data

• dbSNP Id: rs746918765
• gnomAD v3: 6-36676641-C-G
• gnomAD v4: 6-36676641-C-G
• MyVariant Identifiers: chr6:g.36644418C>G (hg19) ; chr6:g.36676641C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.36676641C>G , CM000668.2:g.36676641C>G	GRCh38
NC_000006.11:g.36644418C>G , CM000668.1:g.36644418C>G	GRCh37
NC_000006.10:g.36752396C>G	NCBI36
NG_009364.1:g.2960C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000448526.6:c.-38+117C>G	ENSP00000409259.3:n.-38+117C>G
ENST00000459970.1:n.43+71C>G
ENST00000615513.4:c.-6+117C>G	ENSP00000482768.1:n.-6+117C>G
NM_001220777.1:c.-6+117C>G	NP_001207706.1:n.-6+117C>G
NM_001291549.1:c.-142+71C>G	NP_001278478.1:n.-142+71C>G
NM_078467.2:c.-38+117C>G	NP_510867.1:n.-38+117C>G
NM_001220777.2:c.-6+117C>G	NP_001207706.1:n.-6+117C>G
NM_001291549.3:c.-142+71C>G	NP_001278478.1:n.-142+71C>G
NM_001374509.1:c.-50+71C>G	NP_001361438.1:n.-50+71C>G
NM_001374510.1:c.34+71C>G	NP_001361439.1:n.34+71C>G
NM_078467.3:c.-38+117C>G	NP_510867.1:n.-38+117C>G