Canonical Allele Identifier: CA563688788

Gene: ADAM19

Linked Data

• dbSNP Id: rs1349153842
• gnomAD v2: 5-156942173-G-C
• gnomAD v3: 5-157515165-G-C
• gnomAD v4: 5-157515165-G-C
• MyVariant Identifiers: chr5:g.156942173G>C (hg19) ; chr5:g.157515165G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157515165G>C , CM000667.2:g.157515165G>C	GRCh38
NC_000005.9:g.156942173G>C , CM000667.1:g.156942173G>C	GRCh37
NC_000005.8:g.156874751G>C	NCBI36
NG_046960.1:g.65659C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257527.9:c.667-1660C>G MANE Select	ENSP00000257527.5:n.667-1660C>G
ENST00000257527.8:c.667-1660C>G	ENSP00000257527.4:n.667-1660C>G
ENST00000517905.1:c.667-1660C>G	ENSP00000428654.1:n.667-1660C>G
ENST00000517951.5:c.667-1660C>G	ENSP00000428376.1:n.667-1660C>G
NM_033274.4:c.667-1660C>G	NP_150377.1:n.667-1660C>G
XM_005266003.2:c.667-1660C>G	XP_005266060.1:n.667-1660C>G
XM_011534680.1:c.-135-1660C>G	XP_011532982.1:n.-135-1660C>G
XM_011534681.1:c.-145-1660C>G	XP_011532983.1:n.-145-1660C>G
NM_033274.5:c.667-1660C>G MANE Select	NP_150377.1:n.667-1660C>G