Canonical Allele Identifier: CA130182501

Gene: ADAM19

Linked Data

• dbSNP Id: rs962394604
• MyVariant Identifiers: chr5:g.156970200T>C (hg19) ; chr5:g.157543192T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157543192T>C , CM000667.2:g.157543192T>C	GRCh38
NC_000005.9:g.156970200T>C , CM000667.1:g.156970200T>C	GRCh37
NC_000005.8:g.156902778T>C	NCBI36
NG_046960.1:g.37632A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000257527.9:c.252-5201A>G MANE Select	ENSP00000257527.5:n.252-5201A>G
ENST00000257527.8:c.252-5201A>G	ENSP00000257527.4:n.252-5201A>G
ENST00000517905.1:c.252-5201A>G	ENSP00000428654.1:n.252-5201A>G
ENST00000517951.5:c.252-5201A>G	ENSP00000428376.1:n.252-5201A>G
NM_033274.4:c.252-5201A>G	NP_150377.1:n.252-5201A>G
XM_005266003.2:c.252-5201A>G	XP_005266060.1:n.252-5201A>G
NM_033274.5:c.252-5201A>G MANE Select	NP_150377.1:n.252-5201A>G