Canonical Allele Identifier: CA130185864

Gene: ADAM19

Linked Data

• dbSNP Id: rs1018682532
• MyVariant Identifiers: chr5:g.156945116C>T (hg19) ; chr5:g.157518108C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157518108C>T , CM000667.2:g.157518108C>T	GRCh38
NC_000005.9:g.156945116C>T , CM000667.1:g.156945116C>T	GRCh37
NC_000005.8:g.156877694C>T	NCBI36
NG_046960.1:g.62716G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000257527.9:c.666+715G>A MANE Select	ENSP00000257527.5:n.666+715G>A
ENST00000257527.8:c.666+715G>A	ENSP00000257527.4:n.666+715G>A
ENST00000517905.1:c.666+715G>A	ENSP00000428654.1:n.666+715G>A
ENST00000517951.5:c.666+715G>A	ENSP00000428376.1:n.666+715G>A
NM_033274.4:c.666+715G>A	NP_150377.1:n.666+715G>A
XM_005266003.2:c.666+715G>A	XP_005266060.1:n.666+715G>A
XM_011534680.1:c.-135-4603G>A	XP_011532982.1:n.-135-4603G>A
XM_011534681.1:c.-145-4603G>A	XP_011532983.1:n.-145-4603G>A
NM_033274.5:c.666+715G>A MANE Select	NP_150377.1:n.666+715G>A