Canonical Allele Identifier: CA1217911658

Gene: F13B

Linked Data

• dbSNP Id: rs1655661475
• gnomAD v4: 1-197056951-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197056951T>G , CM000663.2:g.197056951T>G	GRCh38
NC_000001.10:g.197026081T>G , CM000663.1:g.197026081T>G	GRCh37
NC_000001.9:g.195292704T>G	NCBI36
NG_012065.1:g.15317A>C , LRG_550:g.15317A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000367412.2:c.1171+62A>C MANE Select	ENSP00000356382.2:n.1171+62A>C
ENST00000367412.1:c.1171+62A>C	ENSP00000356382.1:n.1171+62A>C
NM_001994.2:c.1171+62A>C , LRG_550t1:c.1171+62A>C	NP_001985.2:n.1171+62A>C
XM_011509283.1:c.1171+62A>C	XP_011507585.1:n.1171+62A>C
XM_011509284.1:c.1168+62A>C	XP_011507586.1:n.1168+62A>C
XM_011509285.1:c.1075+62A>C	XP_011507587.1:n.1075+62A>C
XM_011509286.1:c.1027+62A>C	XP_011507588.1:n.1027+62A>C
XM_011509283.2:c.1171+62A>C	XP_011507585.1:n.1171+62A>C
XM_011509284.2:c.1168+62A>C	XP_011507586.1:n.1168+62A>C
XM_011509286.2:c.1027+62A>C	XP_011507588.1:n.1027+62A>C
NM_001994.3:c.1171+62A>C MANE Select	NP_001985.2:n.1171+62A>C