Canonical Allele Identifier: CA596600754

Gene: ADAM12

Linked Data

• dbSNP Id: rs751472835
• gnomAD v2: 10-127724693-C-A
• gnomAD v4: 10-126036124-C-A
• MyVariant Identifiers: chr10:g.127724693C>A (hg19) ; chr10:g.126036124C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.126036124C>A , CM000672.2:g.126036124C>A	GRCh38
NC_000010.10:g.127724693C>A , CM000672.1:g.127724693C>A	GRCh37
NC_000010.9:g.127714683C>A	NCBI36
NG_029050.1:g.357435G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000448723.2:c.2529+22G>T MANE Select	ENSP00000391268.2:n.2529+22G>T
ENST00000368679.8:c.2538+22G>T	ENSP00000357668.4:n.2538+22G>T
NM_001288973.1:c.2529+22G>T	NP_001275902.1:n.2529+22G>T
NM_003474.5:c.2538+22G>T	NP_003465.3:n.2538+22G>T
XM_017016705.1:c.2070+22G>T	XP_016872194.1:n.2070+22G>T
XM_017016706.1:c.1371+22G>T	XP_016872195.1:n.1371+22G>T
XM_024448210.1:c.1200+22G>T	XP_024303978.1:n.1200+22G>T
NM_001288973.2:c.2529+22G>T MANE Select	NP_001275902.1:n.2529+22G>T
NM_003474.6:c.2538+22G>T	NP_003465.3:n.2538+22G>T