Canonical Allele Identifier: CA130184652

Gene: ADAM19

Linked Data

• dbSNP Id: rs1050474725
• MyVariant Identifiers: chr5:g.156942131A>T (hg19) ; chr5:g.157515123A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157515123A>T , CM000667.2:g.157515123A>T	GRCh38
NC_000005.9:g.156942131A>T , CM000667.1:g.156942131A>T	GRCh37
NC_000005.8:g.156874709A>T	NCBI36
NG_046960.1:g.65701T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000257527.9:c.667-1618T>A MANE Select	ENSP00000257527.5:n.667-1618T>A
ENST00000257527.8:c.667-1618T>A	ENSP00000257527.4:n.667-1618T>A
ENST00000517905.1:c.667-1618T>A	ENSP00000428654.1:n.667-1618T>A
ENST00000517951.5:c.667-1618T>A	ENSP00000428376.1:n.667-1618T>A
NM_033274.4:c.667-1618T>A	NP_150377.1:n.667-1618T>A
XM_005266003.2:c.667-1618T>A	XP_005266060.1:n.667-1618T>A
XM_011534680.1:c.-135-1618T>A	XP_011532982.1:n.-135-1618T>A
XM_011534681.1:c.-145-1618T>A	XP_011532983.1:n.-145-1618T>A
NM_033274.5:c.667-1618T>A MANE Select	NP_150377.1:n.667-1618T>A